ENST00000297784.10:c.1912G>T
MANE Select
|
ENSP00000297784.6:p.Gly638Cys
|
|
ENST00000644967.1:c.*352G>T
|
ENSP00000496159.1:n.*352G>T
|
|
ENST00000645053.1:c.1258-5879G>T
|
ENSP00000493838.1:n.1258-5879G>T
|
|
ENST00000645208.2:c.1912G>T
|
ENSP00000494684.1:p.Gly638Cys
|
|
ENST00000645773.1:c.1786G>T
|
ENSP00000493698.1:p.Gly596Cys
|
|
ENST00000645787.1:n.2055G>T
|
|
|
ENST00000646619.1:c.1474G>T
|
ENSP00000493726.1:p.Gly492Cys
|
|
ENST00000651183.1:c.1474G>T
|
ENSP00000498723.1:p.Gly492Cys
|
|
ENST00000297784.9:c.1912G>T
|
ENSP00000297784.5:p.Gly638Cys
|
|
ENST00000340019.4:c.1912G>T
|
ENSP00000341433.3:p.Gly638Cys
|
|
ENST00000469455.1:n.393G>T
|
|
|
ENST00000486417.5:n.810G>T
|
|
|
NM_138691.2:c.1912G>T
|
NP_619636.2:p.Gly638Cys
|
|
XM_011518213.1:c.2500G>T
|
XP_011516515.1:p.Gly834Cys
|
|
XM_017014256.1:c.1915G>T
|
XP_016869745.1:p.Gly639Cys
|
|
NM_138691.3:c.1912G>T
MANE Select
|
NP_619636.2:p.Gly638Cys
|
|