ENST00000344209.10:c.1122T>A
MANE Select
|
ENSP00000345667.5:p.Pro374=
|
|
ENST00000460554.2:n.1072T>A
|
|
|
ENST00000642615.1:c.*305T>A
|
ENSP00000495499.1:n.*305T>A
|
|
ENST00000273691.7:c.990T>A
|
ENSP00000273691.3:p.Pro330=
|
|
ENST00000344209.9:c.1122T>A
|
ENSP00000345667.5:p.Pro374=
|
|
ENST00000393631.5:c.855T>A
|
ENSP00000377251.1:p.Pro285=
|
|
ENST00000460554.1:n.1224T>A
|
|
|
ENST00000462014.1:c.1026T>A
|
ENSP00000419414.1:p.Pro342=
|
|
NM_001199799.1:c.1122T>A
|
NP_001186728.1:p.Pro374=
|
|
NM_001199800.1:c.855T>A
|
NP_001186729.1:p.Pro285=
|
|
NM_175924.3:c.990T>A
|
NP_787120.1:p.Pro330=
|
|
XM_005247389.3:c.1026T>A
|
XP_005247446.1:p.Pro342=
|
|
XM_011512738.1:c.1122T>A
|
XP_011511040.1:p.Pro374=
|
|
XM_011512739.1:c.585T>A
|
XP_011511041.1:p.Pro195=
|
|
XM_005247389.4:c.1026T>A
|
XP_005247446.1:p.Pro342=
|
|
XM_011512738.2:c.1122T>A
|
XP_011511040.1:p.Pro374=
|
|
XM_011512739.2:c.585T>A
|
XP_011511041.1:p.Pro195=
|
|
NM_001199799.2:c.1122T>A
MANE Select
|
NP_001186728.1:p.Pro374=
|
|
NM_001199800.2:c.855T>A
|
NP_001186729.1:p.Pro285=
|
|
NM_175924.4:c.990T>A
|
NP_787120.1:p.Pro330=
|
|