ENST00000696982.1:c.998G=
|
ENSP00000513017.1:p.Ser333=
|
|
ENST00000527786.7:c.977G=
MANE Select
|
ENSP00000433488.2:p.Ser326=
|
|
ENST00000281428.12:c.779G=
|
ENSP00000281428.8:p.Ser260=
|
|
ENST00000344954.10:c.398G=
|
ENSP00000339627.7:p.Ser133=
|
|
ENST00000429175.7:c.*899G=
|
ENSP00000399985.3:n.*899G=
|
|
ENST00000527786.6:c.977G=
|
ENSP00000433488.2:p.Ser326=
|
|
ENST00000528790.1:n.3560G=
|
|
|
ENST00000534087.3:c.878G=
|
ENSP00000432950.1:p.Ser293=
|
|
ENST00000608303.5:c.*369G=
|
ENSP00000477262.1:n.*369G=
|
|
NM_001167681.2:c.878G=
|
NP_001161153.1:p.Ser293=
|
|
NM_001271010.1:c.779G=
|
NP_001257939.1:p.Ser260=
|
|
NM_001271012.1:c.398G=
|
NP_001257941.1:p.Ser133=
|
|
NM_002017.4:c.977G=
|
NP_002008.2:p.Ser326=
|
|
XM_011542701.1:c.878G=
|
XP_011541003.1:p.Ser293=
|
|
XM_011542702.1:c.851G=
|
XP_011541004.1:p.Ser284=
|
|
XM_011542701.2:c.878G=
|
XP_011541003.1:p.Ser293=
|
|
XM_017017405.1:c.878G=
|
XP_016872894.1:p.Ser293=
|
|
XM_017017406.1:c.878G=
|
XP_016872895.1:p.Ser293=
|
|
NM_002017.5:c.977G=
MANE Select
|
NP_002008.2:p.Ser326=
|
|
NM_001167681.3:c.878G=
|
NP_001161153.1:p.Ser293=
|
|
NM_001271010.2:c.779G=
|
NP_001257939.1:p.Ser260=
|
|
NM_001271012.2:c.398G=
|
NP_001257941.1:p.Ser133=
|
|