ENST00000434127.3:c.874A>T
MANE Select
|
ENSP00000399468.2:p.Thr292Ser
|
|
ENST00000643792.1:n.1556A>T
|
|
|
ENST00000344120.4:c.943A>T
|
ENSP00000344967.4:p.Thr315Ser
|
|
ENST00000434127.2:c.874A>T
|
ENSP00000399468.2:p.Thr292Ser
|
|
NM_001127496.1:c.874A>T
|
NP_001120968.1:p.Thr292Ser
|
|
NM_001293289.1:c.874A>T
|
NP_001280218.1:p.Thr292Ser
|
|
NM_001293290.1:c.874A>T
|
NP_001280219.1:p.Thr292Ser
|
|
NM_030964.3:c.943A>T
|
NP_112226.2:p.Thr315Ser
|
|
XM_011537685.1:c.943A>T
|
XP_011535987.1:p.Thr315Ser
|
|
XM_011537685.3:c.943A>T
|
XP_011535987.1:p.Thr315Ser
|
|
XM_017009910.2:c.874A>T
|
XP_016865399.1:p.Thr292Ser
|
|
NM_001127496.2:c.874A>T
|
NP_001120968.1:p.Thr292Ser
|
|
NM_001293289.2:c.874A>T
|
NP_001280218.1:p.Thr292Ser
|
|
NM_001293290.2:c.874A>T
|
NP_001280219.1:p.Thr292Ser
|
|
NM_030964.4:c.943A>T
|
NP_112226.2:p.Thr315Ser
|
|
NM_001127496.3:c.874A>T
MANE Select
|
NP_001120968.1:p.Thr292Ser
|
|
NM_001293289.3:c.874A>T
|
NP_001280218.1:p.Thr292Ser
|
|
NM_001293290.3:c.874A>T
|
NP_001280219.1:p.Thr292Ser
|
|
NM_030964.5:c.943A>T
|
NP_112226.2:p.Thr315Ser
|
|