ENST00000356839.10:c.1145A>T
MANE Select
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ENSP00000349297.5:p.Lys382Met
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ENST00000322910.9:c.*1100A>T
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ENSP00000325395.5:n.*1100A>T
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|
ENST00000350303.9:c.1079A>T
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ENSP00000344152.5:p.Lys360Met
|
|
ENST00000356839.9:c.1145A>T
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ENSP00000349297.5:p.Lys382Met
|
|
ENST00000542255.6:c.3A>T
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|
|
ENST00000543245.6:c.1214A>T
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ENSP00000438689.2:p.Lys405Met
|
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ENST00000578579.2:n.94A>T
|
|
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ENST00000578824.5:n.561A>T
|
|
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ENST00000579425.5:n.169A>T
|
|
|
ENST00000582379.1:n.796A>T
|
|
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ENST00000583858.5:c.174A>T
|
|
|
ENST00000585203.6:n.353A>T
|
|
|
NM_000018.3:c.1145A>T
|
NP_000009.1:p.Lys382Met
|
|
NM_001033859.2:c.1079A>T
|
NP_001029031.1:p.Lys360Met
|
|
NM_001270447.1:c.1214A>T
|
NP_001257376.1:p.Lys405Met
|
|
NM_001270448.1:c.917A>T
|
NP_001257377.1:p.Lys306Met
|
|
XM_006721516.2:c.1145A>T
|
XP_006721579.2:p.Lys382Met
|
|
XM_011523829.1:c.1145A>T
|
XP_011522131.1:p.Lys382Met
|
|
XM_011523830.1:c.1145A>T
|
XP_011522132.1:p.Lys382Met
|
|
XR_934021.1:n.1252A>T
|
|
|
XR_934022.1:n.1252A>T
|
|
|
XR_934023.1:n.1252A>T
|
|
|
XM_006721516.3:c.1145A>T
|
XP_006721579.2:p.Lys382Met
|
|
XM_011523829.2:c.1145A>T
|
XP_011522131.1:p.Lys382Met
|
|
XM_011523830.2:c.1145A>T
|
XP_011522132.1:p.Lys382Met
|
|
XM_024450741.1:c.1145A>T
|
XP_024306509.1:p.Lys382Met
|
|
XR_934021.2:n.1204A>T
|
|
|
XR_934022.2:n.1204A>T
|
|
|
XR_934023.2:n.1204A>T
|
|
|
NM_000018.4:c.1145A>T
MANE Select
|
NP_000009.1:p.Lys382Met
|
|
NM_001033859.3:c.1079A>T
|
NP_001029031.1:p.Lys360Met
|
|
NM_001270447.2:c.1214A>T
|
NP_001257376.1:p.Lys405Met
|
|
NM_001270448.2:c.917A>T
|
NP_001257377.1:p.Lys306Met
|
|