|
NM_000215.4:c.1744C>T
MANE Select
|
NP_000206.2:p.Arg582Trp
|
|
ENST00000458235.7:c.1744C>T
MANE Select
|
ENSP00000391676.1:p.Arg582Trp
|
|
NM_000215.3:c.1744C>T , LRG_77t1:c.1744C>T
|
NP_000206.2:p.Arg582Trp
|
|
ENST00000458235.5:c.1744C>T
|
ENSP00000391676.1:p.Arg582Trp
|
|
ENST00000526008.6:c.*301C>T
|
ENSP00000513006.1:n.*301C>T
|
|
ENST00000527031.5:n.1834C>T
|
|
|
ENST00000527670.5:c.1744C>T
|
ENSP00000432511.1:p.Arg582Trp
|
|
ENST00000534444.1:c.1744C>T
|
ENSP00000436421.1:p.Arg582Trp
|
|
ENST00000696967.1:n.921C>T
|
|
|
ENST00000696970.1:n.399C>T
|
|
|
XM_005259896.2:c.1873C>T
|
XP_005259953.1:p.Arg625Trp
|
|
XM_005259896.3:c.1873C>T
|
XP_005259953.1:p.Arg625Trp
|
|
XM_006722745.2:c.1744C>T
|
XP_006722808.1:p.Arg582Trp
|
|
XM_011527990.1:c.1873C>T
|
XP_011526292.1:p.Arg625Trp
|
|
XM_011527991.1:c.1873C>T
|
XP_011526293.1:p.Arg625Trp
|
|
XM_011527991.2:c.1873C>T
|
XP_011526293.1:p.Arg625Trp
|
|
XR_430137.2:n.1883C>T
|
|
