ENST00000530449.2:n.153G>T
|
|
|
ENST00000698254.1:c.1057G>T
|
ENSP00000513629.1:p.Gly353Ter
|
|
ENST00000698255.1:c.1477G>T
|
ENSP00000513630.1:p.Gly493Ter
|
|
ENST00000698256.1:c.994G>T
|
|
|
ENST00000698257.1:n.946G>T
|
|
|
ENST00000698258.1:n.663G>T
|
|
|
ENST00000698259.1:n.429G>T
|
|
|
ENST00000265686.8:c.1528G>T
MANE Select
|
ENSP00000265686.3:p.Gly510Ter
|
|
ENST00000265686.7:c.1528G>T
|
ENSP00000265686.3:p.Gly510Ter
|
|
ENST00000525516.1:n.322G>T
|
|
|
ENST00000525724.5:n.840G>T
|
|
|
ENST00000528981.5:c.680G>T
|
|
|
ENST00000532635.5:c.880G>T
|
ENSP00000434407.1:p.Gly294Ter
|
|
ENST00000533005.5:n.641G>T
|
|
|
NM_006019.3:c.1528G>T
|
NP_006010.2:p.Gly510Ter
|
|
NM_006053.3:c.880G>T
|
NP_006044.1:p.Gly294Ter
|
|
XM_005273709.2:c.1528G>T
|
XP_005273766.1:p.Gly510Ter
|
|
XM_011544726.1:c.1528G>T
|
XP_011543028.1:p.Gly510Ter
|
|
XM_011544727.1:c.1528G>T
|
XP_011543029.1:p.Gly510Ter
|
|
XM_011544728.1:c.1528G>T
|
XP_011543030.1:p.Gly510Ter
|
|
XR_949754.1:n.1532G>T
|
|
|
NM_001351059.1:c.634G>T
|
NP_001337988.1:p.Gly212Ter
|
|
XM_024448320.1:c.1621G>T
|
XP_024304088.1:p.Gly541Ter
|
|
XM_024448321.1:c.1621G>T
|
XP_024304089.1:p.Gly541Ter
|
|
XM_024448322.1:c.1621G>T
|
XP_024304090.1:p.Gly541Ter
|
|
XM_024448323.1:c.1621G>T
|
XP_024304091.1:p.Gly541Ter
|
|
XM_024448324.1:c.1621G>T
|
XP_024304092.1:p.Gly541Ter
|
|
XR_001747721.2:n.1652G>T
|
|
|
XR_001747722.1:n.1665G>T
|
|
|
XR_001747723.2:n.1665G>T
|
|
|
XR_002957115.1:n.1743G>T
|
|
|
NM_006019.4:c.1528G>T
MANE Select
|
NP_006010.2:p.Gly510Ter
|
|
NM_001351059.2:c.634G>T
|
NP_001337988.1:p.Gly212Ter
|
|
NM_006053.4:c.880G>T
|
NP_006044.1:p.Gly294Ter
|
|