ENST00000295408.9:c.665G>T
MANE Select
|
ENSP00000295408.4:p.Gly222Val
|
|
ENST00000295408.8:c.665G>T
|
ENSP00000295408.4:p.Gly222Val
|
|
ENST00000409780.5:c.137G>T
|
ENSP00000387277.1:p.Gly46Val
|
|
ENST00000421804.6:c.665G>T
|
ENSP00000389152.2:p.Gly222Val
|
|
ENST00000439966.5:c.*138G>T
|
ENSP00000402129.1:n.*138G>T
|
|
ENST00000616902.4:c.-551G>T
|
ENSP00000482824.1:n.-551G>T
|
|
NM_006343.2:c.665G>T
|
NP_006334.2:p.Gly222Val
|
|
XM_005263565.3:c.665G>T
|
XP_005263622.1:p.Gly222Val
|
|
XM_005263568.3:c.665G>T
|
XP_005263625.1:p.Gly222Val
|
|
XM_011510490.1:c.476G>T
|
XP_011508792.1:p.Gly159Val
|
|
XM_005263565.4:c.665G>T
|
XP_005263622.1:p.Gly222Val
|
|
XM_005263568.4:c.665G>T
|
XP_005263625.1:p.Gly222Val
|
|
XM_011510490.3:c.476G>T
|
XP_011508792.1:p.Gly159Val
|
|
XM_017003164.1:c.476G>T
|
XP_016858653.1:p.Gly159Val
|
|
XM_017003165.2:c.-603G>T
|
XP_016858654.1:n.-603G>T
|
|
NM_006343.3:c.665G>T
MANE Select
|
NP_006334.2:p.Gly222Val
|
|