ENST00000356839.10:c.1180G>T
MANE Select
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ENSP00000349297.5:p.Glu394Ter
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ENST00000322910.9:c.*1135G>T
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ENSP00000325395.5:n.*1135G>T
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ENST00000350303.9:c.1114G>T
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ENSP00000344152.5:p.Glu372Ter
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ENST00000356839.9:c.1180G>T
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ENSP00000349297.5:p.Glu394Ter
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ENST00000542255.6:c.38G>T
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ENST00000543245.6:c.1249G>T
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ENSP00000438689.2:p.Glu417Ter
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ENST00000578579.2:n.129G>T
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ENST00000578824.5:n.596G>T
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ENST00000579425.5:n.204G>T
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ENST00000579546.1:c.17G>T
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ENST00000582379.1:n.831G>T
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ENST00000583858.5:c.209G>T
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ENST00000585203.6:n.388G>T
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NM_000018.3:c.1180G>T
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NP_000009.1:p.Glu394Ter
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NM_001033859.2:c.1114G>T
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NP_001029031.1:p.Glu372Ter
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NM_001270447.1:c.1249G>T
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NP_001257376.1:p.Glu417Ter
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NM_001270448.1:c.952G>T
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NP_001257377.1:p.Glu318Ter
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XM_006721516.2:c.1180G>T
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XP_006721579.2:p.Glu394Ter
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XM_011523829.1:c.1180G>T
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XP_011522131.1:p.Glu394Ter
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XM_011523830.1:c.1180G>T
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XP_011522132.1:p.Glu394Ter
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XR_934021.1:n.1287G>T
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XR_934022.1:n.1287G>T
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XR_934023.1:n.1287G>T
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XM_006721516.3:c.1180G>T
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XP_006721579.2:p.Glu394Ter
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XM_011523829.2:c.1180G>T
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XP_011522131.1:p.Glu394Ter
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XM_011523830.2:c.1180G>T
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XP_011522132.1:p.Glu394Ter
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XM_024450741.1:c.1180G>T
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XP_024306509.1:p.Glu394Ter
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XR_934021.2:n.1239G>T
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XR_934022.2:n.1239G>T
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XR_934023.2:n.1239G>T
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NM_000018.4:c.1180G>T
MANE Select
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NP_000009.1:p.Glu394Ter
|
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NM_001033859.3:c.1114G>T
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NP_001029031.1:p.Glu372Ter
|
|
NM_001270447.2:c.1249G>T
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NP_001257376.1:p.Glu417Ter
|
|
NM_001270448.2:c.952G>T
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NP_001257377.1:p.Glu318Ter
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