ENST00000696170.1:c.*94A>G
|
ENSP00000512461.1:n.*94A>G
|
|
ENST00000696171.1:c.489A>G
|
ENSP00000512462.1:p.Lys163=
|
|
ENST00000696172.1:c.338-2903A>G
|
ENSP00000512463.1:n.338-2903A>G
|
|
ENST00000378588.5:c.585A>G
MANE Select
|
ENSP00000367851.4:p.Lys195=
|
|
ENST00000378588.4:c.585A>G
|
ENSP00000367851.4:p.Lys195=
|
|
ENST00000465127.1:c.171+370052A>G
|
ENSP00000417050.1:n.171+370052A>G
|
|
NM_000397.3:c.585A>G , LRG_53t1:c.585A>G
|
NP_000388.2:p.Lys195=
|
|
XM_011543890.1:c.279A>G
|
XP_011542192.1:p.Lys93=
|
|
NM_000397.4:c.585A>G
MANE Select
|
NP_000388.2:p.Lys195=
|
|