ENST00000616995.5:n.1566G>T
|
|
|
ENST00000691517.1:n.1079G>T
|
|
|
ENST00000331968.11:c.1795G>T
MANE Select
|
ENSP00000333568.6:p.Gly599Ter
|
|
ENST00000651571.1:c.1607G>T
|
ENSP00000498919.1:n.1607G>T
|
|
ENST00000651616.1:c.1676G>T
|
ENSP00000498661.1:n.1676G>T
|
|
ENST00000331968.9:c.1795G>T
|
ENSP00000333568.5:p.Gly599Ter
|
|
ENST00000415220.6:c.1819G>T
|
ENSP00000390535.2:p.Gly607Ter
|
|
ENST00000616995.4:c.1795G>T
|
ENSP00000482645.1:p.Gly599Ter
|
|
NM_002742.2:c.1795G>T
|
NP_002733.2:p.Gly599Ter
|
|
XM_005267859.1:c.1819G>T
|
XP_005267916.1:p.Gly607Ter
|
|
XM_011536964.1:c.1591G>T
|
XP_011535266.1:p.Gly531Ter
|
|
XM_011536965.1:c.1531G>T
|
XP_011535267.1:p.Gly511Ter
|
|
XR_943493.1:n.1934G>T
|
|
|
NM_001330069.1:c.1819G>T
|
NP_001316998.1:p.Gly607Ter
|
|
NM_001348390.1:c.1531G>T
|
NP_001335319.1:p.Gly511Ter
|
|
XM_011536965.2:c.1531G>T
|
XP_011535267.1:p.Gly511Ter
|
|
XM_017021462.1:c.1300G>T
|
XP_016876951.1:p.Gly434Ter
|
|
XR_943493.2:n.2112G>T
|
|
|
NM_001330069.2:c.1819G>T
|
NP_001316998.1:p.Gly607Ter
|
|
NM_002742.3:c.1795G>T
MANE Select
|
NP_002733.2:p.Gly599Ter
|
|