ENST00000352511.5:c.1295T>C
MANE Select
|
ENSP00000340361.3:p.Val432Ala
|
|
ENST00000352511.4:c.1295T>C
|
ENSP00000340361.3:p.Val432Ala
|
|
ENST00000461232.1:n.5084T>C
|
|
|
ENST00000465020.5:n.1381T>C
|
|
|
NM_001106.3:c.1295T>C
|
NP_001097.2:p.Val432Ala
|
|
XM_005265583.2:c.1358T>C
|
XP_005265640.1:p.Val453Ala
|
|
XM_005265583.3:c.1358T>C
|
XP_005265640.1:p.Val453Ala
|
|
XM_017007514.1:c.1337T>C
|
XP_016863003.1:p.Val446Ala
|
|
XM_017007515.2:c.1313T>C
|
XP_016863004.1:p.Val438Ala
|
|
XM_017007516.1:c.1292T>C
|
XP_016863005.1:p.Val431Ala
|
|
NM_001106.4:c.1295T>C
MANE Select
|
NP_001097.2:p.Val432Ala
|
|