ENST00000368985.8:c.913G>C
MANE Select
|
ENSP00000357981.3:p.Gly305Arg
|
|
ENST00000448301.7:c.685G>C
|
ENSP00000408414.2:p.Gly229Arg
|
|
ENST00000472977.7:c.913G>C
|
ENSP00000475176.2:p.Gly305Arg
|
|
ENST00000483930.2:c.*107G>C
|
ENSP00000475812.2:n.*107G>C
|
|
ENST00000607427.2:c.913G>C
|
ENSP00000475557.2:p.Gly305Arg
|
|
ENST00000679512.1:c.810G>C
|
ENSP00000505113.1:p.Leu270Phe
|
|
ENST00000679898.1:c.640G>C
|
ENSP00000505326.1:p.Gly214Arg
|
|
ENST00000680288.1:c.763G>C
|
ENSP00000506001.1:p.Gly255Arg
|
|
ENST00000680311.1:c.644G>C
|
ENSP00000505020.1:p.Trp215Ser
|
|
ENST00000680471.1:c.*84G>C
|
ENSP00000506603.1:n.*84G>C
|
|
ENST00000680664.1:c.736G>C
|
ENSP00000506248.1:p.Gly246Arg
|
|
ENST00000680931.1:c.*263G>C
|
ENSP00000504934.1:n.*263G>C
|
|
ENST00000681357.1:n.303G>C
|
|
|
ENST00000681444.1:c.913G>C
|
ENSP00000505359.1:p.Gly305Arg
|
|
ENST00000368985.7:c.913G>C
|
ENSP00000357981.3:p.Gly305Arg
|
|
ENST00000448301.6:c.763G>C
|
ENSP00000408414.1:p.Gly255Arg
|
|
ENST00000472977.6:c.206G>C
|
|
|
ENST00000483930.1:c.461G>C
|
ENSP00000475812.1:n.461G>C
|
|
NM_001199739.1:c.763G>C
|
NP_001186668.1:p.Gly255Arg
|
|
NM_004079.4:c.913G>C
|
NP_004070.3:p.Gly305Arg
|
|
NM_004079.5:c.913G>C
MANE Select
|
NP_004070.3:p.Gly305Arg
|
|
NM_001199739.2:c.763G>C
|
NP_001186668.1:p.Gly255Arg
|
|