ENST00000696170.1:c.*144T>G
|
ENSP00000512461.1:n.*144T>G
|
|
ENST00000696171.1:c.539T>G
|
ENSP00000512462.1:p.Phe180Cys
|
|
ENST00000696172.1:c.338-2853T>G
|
ENSP00000512463.1:n.338-2853T>G
|
|
ENST00000378588.5:c.635T>G
MANE Select
|
ENSP00000367851.4:p.Phe212Cys
|
|
ENST00000378588.4:c.635T>G
|
ENSP00000367851.4:p.Phe212Cys
|
|
ENST00000465127.1:c.171+370102T>G
|
ENSP00000417050.1:n.171+370102T>G
|
|
NM_000397.3:c.635T>G , LRG_53t1:c.635T>G
|
NP_000388.2:p.Phe212Cys
|
|
XM_011543890.1:c.329T>G
|
XP_011542192.1:p.Phe110Cys
|
|
NM_000397.4:c.635T>G
MANE Select
|
NP_000388.2:p.Phe212Cys
|
|