ENST00000696170.1:c.*2G>C
|
ENSP00000512461.1:n.*2G>C
|
|
ENST00000696171.1:c.397G>C
|
ENSP00000512462.1:p.Gly133Arg
|
|
ENST00000696172.1:c.338-2995G>C
|
ENSP00000512463.1:n.338-2995G>C
|
|
ENST00000378588.5:c.493G>C
MANE Select
|
ENSP00000367851.4:p.Gly165Arg
|
|
ENST00000378588.4:c.493G>C
|
ENSP00000367851.4:p.Gly165Arg
|
|
ENST00000465127.1:c.171+369960G>C
|
ENSP00000417050.1:n.171+369960G>C
|
|
NM_000397.3:c.493G>C , LRG_53t1:c.493G>C
|
NP_000388.2:p.Gly165Arg
|
|
XM_011543890.1:c.187G>C
|
XP_011542192.1:p.Gly63Arg
|
|
NM_000397.4:c.493G>C
MANE Select
|
NP_000388.2:p.Gly165Arg
|
|