ENST00000328300.11:c.4493T>C
MANE Select
|
ENSP00000331902.7:p.Val1498Ala
|
|
ENST00000361603.7:c.4475T>C
|
ENSP00000354505.2:p.Val1492Ala
|
|
ENST00000510690.2:n.987T>C
|
|
|
ENST00000328300.10:c.4493T>C
|
ENSP00000331902.6:p.Val1498Ala
|
|
ENST00000361603.6:c.4475T>C
|
ENSP00000354505.2:p.Val1492Ala
|
|
ENST00000515658.1:c.289T>C
|
|
|
NM_000495.4:c.4475T>C
|
NP_000486.1:p.Val1492Ala
|
|
NM_033380.2:c.4493T>C
|
NP_203699.1:p.Val1498Ala
|
|
XM_005262070.2:c.4484T>C
|
XP_005262127.1:p.Val1495Ala
|
|
XM_006724616.2:c.4493T>C
|
XP_006724679.1:p.Val1498Ala
|
|
XM_011530849.1:c.4169T>C
|
XP_011529151.1:p.Val1390Ala
|
|
XM_011530851.1:c.2066T>C
|
XP_011529153.1:p.Val689Ala
|
|
XM_011530849.2:c.4508T>C
|
XP_011529151.2:p.Val1503Ala
|
|
XM_017029259.2:c.4499T>C
|
XP_016884748.1:p.Val1500Ala
|
|
XM_017029260.1:c.4490T>C
|
XP_016884749.1:p.Val1497Ala
|
|
XM_017029263.2:c.2828T>C
|
XP_016884752.1:p.Val943Ala
|
|
NM_000495.5:c.4475T>C
|
NP_000486.1:p.Val1492Ala
|
|
NM_033380.3:c.4493T>C
MANE Select
|
NP_203699.1:p.Val1498Ala
|
|