ENST00000696170.1:c.*494T>C
|
ENSP00000512461.1:n.*494T>C
|
|
ENST00000696171.1:c.889T>C
|
ENSP00000512462.1:p.Cys297Arg
|
|
ENST00000378588.5:c.985T>C
MANE Select
|
ENSP00000367851.4:p.Cys329Arg
|
|
ENST00000378588.4:c.985T>C
|
ENSP00000367851.4:p.Cys329Arg
|
|
ENST00000465127.1:c.171+377964T>C
|
ENSP00000417050.1:n.171+377964T>C
|
|
ENST00000492288.1:n.410T>C
|
|
|
NM_000397.3:c.985T>C , LRG_53t1:c.985T>C
|
NP_000388.2:p.Cys329Arg
|
|
XM_011543890.1:c.679T>C
|
XP_011542192.1:p.Cys227Arg
|
|
NM_000397.4:c.985T>C
MANE Select
|
NP_000388.2:p.Cys329Arg
|
|