ENST00000696170.1:c.*244A>C
|
ENSP00000512461.1:n.*244A>C
|
|
ENST00000696171.1:c.639A>C
|
ENSP00000512462.1:p.Glu213Asp
|
|
ENST00000696172.1:c.*11A>C
|
ENSP00000512463.1:n.*11A>C
|
|
ENST00000378588.5:c.735A>C
MANE Select
|
ENSP00000367851.4:p.Glu245Asp
|
|
ENST00000378588.4:c.735A>C
|
ENSP00000367851.4:p.Glu245Asp
|
|
ENST00000465127.1:c.171+373015A>C
|
ENSP00000417050.1:n.171+373015A>C
|
|
ENST00000492288.1:n.160A>C
|
|
|
NM_000397.3:c.735A>C , LRG_53t1:c.735A>C
|
NP_000388.2:p.Glu245Asp
|
|
XM_011543890.1:c.429A>C
|
XP_011542192.1:p.Glu143Asp
|
|
NM_000397.4:c.735A>C
MANE Select
|
NP_000388.2:p.Glu245Asp
|
|