ENST00000281928.9:c.3356T>C
MANE Select
|
ENSP00000281928.3:p.Val1119Ala
|
|
ENST00000549786.2:c.2784T>C
|
|
|
ENST00000648379.1:n.1724T>C
|
|
|
ENST00000648737.1:n.3120T>C
|
|
|
ENST00000648825.1:n.96T>C
|
|
|
ENST00000648916.1:n.1367T>C
|
|
|
ENST00000649607.1:c.1540T>C
|
|
|
ENST00000650226.1:c.3356T>C
|
ENSP00000496981.1:p.Val1119Ala
|
|
ENST00000281928.7:c.3356T>C
|
ENSP00000281928.3:p.Val1119Ala
|
|
NM_015335.4:c.3356T>C
|
NP_056150.1:p.Val1119Ala
|
|
XM_011538080.1:c.3356T>C
|
XP_011536382.1:p.Val1119Ala
|
|
XM_011538081.1:c.3353T>C
|
XP_011536383.1:p.Val1118Ala
|
|
XM_011538082.1:c.3326T>C
|
XP_011536384.1:p.Val1109Ala
|
|
XM_011538080.2:c.3356T>C
|
XP_011536382.1:p.Val1119Ala
|
|
XM_011538081.2:c.3353T>C
|
XP_011536383.1:p.Val1118Ala
|
|
XM_011538082.2:c.3326T>C
|
XP_011536384.1:p.Val1109Ala
|
|
XM_017019090.1:c.3353T>C
|
XP_016874579.1:p.Val1118Ala
|
|
NM_015335.5:c.3356T>C
MANE Select
|
NP_056150.1:p.Val1119Ala
|
|