ENST00000344209.10:c.1028G>C
MANE Select
|
ENSP00000345667.5:p.Arg343Thr
|
|
ENST00000460554.2:n.978G>C
|
|
|
ENST00000642615.1:c.*211G>C
|
ENSP00000495499.1:n.*211G>C
|
|
ENST00000273691.7:c.896G>C
|
ENSP00000273691.3:p.Arg299Thr
|
|
ENST00000344209.9:c.1028G>C
|
ENSP00000345667.5:p.Arg343Thr
|
|
ENST00000393631.5:c.761G>C
|
ENSP00000377251.1:p.Arg254Thr
|
|
ENST00000460554.1:n.1130G>C
|
|
|
ENST00000462014.1:c.932G>C
|
ENSP00000419414.1:p.Arg311Thr
|
|
NM_001199799.1:c.1028G>C
|
NP_001186728.1:p.Arg343Thr
|
|
NM_001199800.1:c.761G>C
|
NP_001186729.1:p.Arg254Thr
|
|
NM_175924.3:c.896G>C
|
NP_787120.1:p.Arg299Thr
|
|
XM_005247389.3:c.932G>C
|
XP_005247446.1:p.Arg311Thr
|
|
XM_011512738.1:c.1028G>C
|
XP_011511040.1:p.Arg343Thr
|
|
XM_011512739.1:c.491G>C
|
XP_011511041.1:p.Arg164Thr
|
|
XM_005247389.4:c.932G>C
|
XP_005247446.1:p.Arg311Thr
|
|
XM_011512738.2:c.1028G>C
|
XP_011511040.1:p.Arg343Thr
|
|
XM_011512739.2:c.491G>C
|
XP_011511041.1:p.Arg164Thr
|
|
NM_001199799.2:c.1028G>C
MANE Select
|
NP_001186728.1:p.Arg343Thr
|
|
NM_001199800.2:c.761G>C
|
NP_001186729.1:p.Arg254Thr
|
|
NM_175924.4:c.896G>C
|
NP_787120.1:p.Arg299Thr
|
|