ENST00000616995.5:n.1539G>T
|
|
|
ENST00000691517.1:n.1052G>T
|
|
|
ENST00000331968.11:c.1768G>T
MANE Select
|
ENSP00000333568.6:p.Gly590Cys
|
|
ENST00000651571.1:c.1580G>T
|
ENSP00000498919.1:n.1580G>T
|
|
ENST00000651616.1:c.1649G>T
|
ENSP00000498661.1:n.1649G>T
|
|
ENST00000331968.9:c.1768G>T
|
ENSP00000333568.5:p.Gly590Cys
|
|
ENST00000415220.6:c.1792G>T
|
ENSP00000390535.2:p.Gly598Cys
|
|
ENST00000616995.4:c.1768G>T
|
ENSP00000482645.1:p.Gly590Cys
|
|
NM_002742.2:c.1768G>T
|
NP_002733.2:p.Gly590Cys
|
|
XM_005267859.1:c.1792G>T
|
XP_005267916.1:p.Gly598Cys
|
|
XM_011536964.1:c.1564G>T
|
XP_011535266.1:p.Gly522Cys
|
|
XM_011536965.1:c.1504G>T
|
XP_011535267.1:p.Gly502Cys
|
|
XR_943493.1:n.1907G>T
|
|
|
NM_001330069.1:c.1792G>T
|
NP_001316998.1:p.Gly598Cys
|
|
NM_001348390.1:c.1504G>T
|
NP_001335319.1:p.Gly502Cys
|
|
XM_011536965.2:c.1504G>T
|
XP_011535267.1:p.Gly502Cys
|
|
XM_017021462.1:c.1273G>T
|
XP_016876951.1:p.Gly425Cys
|
|
XR_943493.2:n.2085G>T
|
|
|
NM_001330069.2:c.1792G>T
|
NP_001316998.1:p.Gly598Cys
|
|
NM_002742.3:c.1768G>T
MANE Select
|
NP_002733.2:p.Gly590Cys
|
|