ENST00000344209.10:c.1356C>A
MANE Select
|
ENSP00000345667.5:p.Pro452=
|
|
ENST00000460554.2:n.1306C>A
|
|
|
ENST00000642615.1:c.*539C>A
|
ENSP00000495499.1:n.*539C>A
|
|
ENST00000273691.7:c.1224C>A
|
ENSP00000273691.3:p.Pro408=
|
|
ENST00000344209.9:c.1356C>A
|
ENSP00000345667.5:p.Pro452=
|
|
ENST00000393631.5:c.1089C>A
|
ENSP00000377251.1:p.Pro363=
|
|
ENST00000460554.1:n.1458C>A
|
|
|
ENST00000462014.1:c.1260C>A
|
ENSP00000419414.1:p.Pro420=
|
|
NM_001199799.1:c.1356C>A
|
NP_001186728.1:p.Pro452=
|
|
NM_001199800.1:c.1089C>A
|
NP_001186729.1:p.Pro363=
|
|
NM_175924.3:c.1224C>A
|
NP_787120.1:p.Pro408=
|
|
XM_005247389.3:c.1260C>A
|
XP_005247446.1:p.Pro420=
|
|
XM_011512738.1:c.1356C>A
|
XP_011511040.1:p.Pro452=
|
|
XM_011512739.1:c.819C>A
|
XP_011511041.1:p.Pro273=
|
|
XM_005247389.4:c.1260C>A
|
XP_005247446.1:p.Pro420=
|
|
XM_011512738.2:c.1356C>A
|
XP_011511040.1:p.Pro452=
|
|
XM_011512739.2:c.819C>A
|
XP_011511041.1:p.Pro273=
|
|
NM_001199799.2:c.1356C>A
MANE Select
|
NP_001186728.1:p.Pro452=
|
|
NM_001199800.2:c.1089C>A
|
NP_001186729.1:p.Pro363=
|
|
NM_175924.4:c.1224C>A
|
NP_787120.1:p.Pro408=
|
|