ENST00000356839.10:c.1314G>C
MANE Select
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ENSP00000349297.5:p.Gly438=
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ENST00000322910.9:c.*1269G>C
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ENSP00000325395.5:n.*1269G>C
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ENST00000350303.9:c.1248G>C
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ENSP00000344152.5:p.Gly416=
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ENST00000356839.9:c.1314G>C
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ENSP00000349297.5:p.Gly438=
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ENST00000542255.6:c.172G>C
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ENST00000543245.6:c.1383G>C
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ENSP00000438689.2:p.Gly461=
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ENST00000578711.1:n.353G>C
|
|
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ENST00000579425.5:n.338G>C
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|
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ENST00000579546.1:c.151G>C
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ENST00000583074.5:n.33G>C
|
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ENST00000583850.5:n.89G>C
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ENST00000583858.5:c.343G>C
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|
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ENST00000585203.6:n.522G>C
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|
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NM_000018.3:c.1314G>C
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NP_000009.1:p.Gly438=
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NM_001033859.2:c.1248G>C
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NP_001029031.1:p.Gly416=
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NM_001270447.1:c.1383G>C
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NP_001257376.1:p.Gly461=
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NM_001270448.1:c.1086G>C
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NP_001257377.1:p.Gly362=
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XM_006721516.2:c.1314G>C
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XP_006721579.2:p.Gly438=
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XM_011523829.1:c.1314G>C
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XP_011522131.1:p.Gly438=
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XM_011523830.1:c.1314G>C
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XP_011522132.1:p.Gly438=
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XR_934021.1:n.1421G>C
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XR_934022.1:n.1421G>C
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XR_934023.1:n.1421G>C
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XM_006721516.3:c.1314G>C
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XP_006721579.2:p.Gly438=
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XM_011523829.2:c.1314G>C
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XP_011522131.1:p.Gly438=
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XM_011523830.2:c.1314G>C
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XP_011522132.1:p.Gly438=
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XM_024450741.1:c.1314G>C
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XP_024306509.1:p.Gly438=
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XR_934021.2:n.1373G>C
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XR_934022.2:n.1373G>C
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XR_934023.2:n.1373G>C
|
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NM_000018.4:c.1314G>C
MANE Select
|
NP_000009.1:p.Gly438=
|
|
NM_001033859.3:c.1248G>C
|
NP_001029031.1:p.Gly416=
|
|
NM_001270447.2:c.1383G>C
|
NP_001257376.1:p.Gly461=
|
|
NM_001270448.2:c.1086G>C
|
NP_001257377.1:p.Gly362=
|
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