ENST00000422737.7:c.4457T>C
|
ENSP00000415650.3:p.Val1486Ala
|
|
ENST00000457135.2:c.666T>C
|
|
|
ENST00000334344.11:c.4457T>C
MANE Select
|
ENSP00000335044.6:p.Val1486Ala
|
|
ENST00000422737.6:c.4378T>C
|
|
|
ENST00000334344.10:c.4457T>C
|
ENSP00000335044.6:p.Val1486Ala
|
|
ENST00000422737.5:c.4010T>C
|
ENSP00000415650.1:p.Val1337Ala
|
|
ENST00000444670.5:c.3287T>C
|
ENSP00000397307.1:p.Val1096Ala
|
|
ENST00000457135.1:c.281T>C
|
ENSP00000388357.1:p.Val94Ala
|
|
ENST00000479608.5:n.3748T>C
|
|
|
NM_152641.2:c.4457T>C
|
NP_689854.2:p.Val1486Ala
|
|
XM_006719272.2:c.4457T>C
|
XP_006719335.1:p.Val1486Ala
|
|
XM_011538025.1:c.2825T>C
|
XP_011536327.1:p.Val942Ala
|
|
XR_944505.1:n.4605T>C
|
|
|
NM_001347839.1:c.4457T>C
|
NP_001334768.1:p.Val1486Ala
|
|
NM_152641.3:c.4457T>C
|
NP_689854.2:p.Val1486Ala
|
|
XM_006719272.4:c.4457T>C
|
XP_006719335.1:p.Val1486Ala
|
|
XR_944505.3:n.4588T>C
|
|
|
NM_152641.4:c.4457T>C
MANE Select
|
NP_689854.2:p.Val1486Ala
|
|
NM_001347839.2:c.4457T>C
|
NP_001334768.1:p.Val1486Ala
|
|