ENST00000696170.1:c.211G>T
|
ENSP00000512461.1:p.Val71Phe
|
|
ENST00000696171.1:c.115G>T
|
ENSP00000512462.1:p.Val39Phe
|
|
ENST00000696172.1:c.211G>T
|
ENSP00000512463.1:p.Val71Phe
|
|
ENST00000696173.1:n.219G>T
|
|
|
ENST00000378588.5:c.211G>T
MANE Select
|
ENSP00000367851.4:p.Val71Phe
|
|
ENST00000378588.4:c.211G>T
|
ENSP00000367851.4:p.Val71Phe
|
|
ENST00000465127.1:c.171+357559G>T
|
ENSP00000417050.1:n.171+357559G>T
|
|
NM_000397.3:c.211G>T , LRG_53t1:c.211G>T
|
NP_000388.2:p.Val71Phe
|
|
XM_011543890.1:c.-220G>T
|
XP_011542192.1:n.-220G>T
|
|
NM_000397.4:c.211G>T
MANE Select
|
NP_000388.2:p.Val71Phe
|
|