ENST00000696170.1:c.*121C>G
|
ENSP00000512461.1:n.*121C>G
|
|
ENST00000696171.1:c.516C>G
|
ENSP00000512462.1:p.Val172=
|
|
ENST00000696172.1:c.338-2876C>G
|
ENSP00000512463.1:n.338-2876C>G
|
|
ENST00000378588.5:c.612C>G
MANE Select
|
ENSP00000367851.4:p.Val204=
|
|
ENST00000378588.4:c.612C>G
|
ENSP00000367851.4:p.Val204=
|
|
ENST00000465127.1:c.171+370079C>G
|
ENSP00000417050.1:n.171+370079C>G
|
|
NM_000397.3:c.612C>G , LRG_53t1:c.612C>G
|
NP_000388.2:p.Val204=
|
|
XM_011543890.1:c.306C>G
|
XP_011542192.1:p.Val102=
|
|
NM_000397.4:c.612C>G
MANE Select
|
NP_000388.2:p.Val204=
|
|