ENST00000334504.12:c.4873G>T
MANE Select
|
ENSP00000334733.7:p.Glu1625Ter
|
|
ENST00000334504.11:c.4873G>T
|
ENSP00000334733.7:p.Glu1625Ter
|
|
ENST00000372216.8:c.4876G>T
|
ENSP00000361290.4:p.Glu1626Ter
|
|
ENST00000394872.6:c.4924G>T
|
ENSP00000378340.3:p.Glu1642Ter
|
|
ENST00000538570.5:c.4702G>T
|
ENSP00000445236.1:p.Glu1568Ter
|
|
ENST00000545689.2:c.4837G>T
|
ENSP00000443707.2:p.Glu1613Ter
|
|
ENST00000621266.4:c.4801G>T
|
ENSP00000482970.1:p.Glu1601Ter
|
|
NM_001287758.1:c.4924G>T
|
NP_001274687.1:p.Glu1642Ter
|
|
NM_001287759.1:c.4801G>T
|
NP_001274688.1:p.Glu1601Ter
|
|
NM_001287760.1:c.4702G>T
|
NP_001274689.1:p.Glu1568Ter
|
|
NM_001847.3:c.4876G>T
|
NP_001838.2:p.Glu1626Ter
|
|
NM_033641.3:c.4873G>T
|
NP_378667.1:p.Glu1625Ter
|
|
XM_006724617.2:c.4927G>T
|
XP_006724680.1:p.Glu1643Ter
|
|
XM_011530852.1:c.4855G>T
|
XP_011529154.1:p.Glu1619Ter
|
|
XM_011530853.1:c.4843G>T
|
XP_011529155.1:p.Glu1615Ter
|
|
XM_006724617.3:c.4927G>T
|
XP_006724680.1:p.Glu1643Ter
|
|
XM_011530852.2:c.4855G>T
|
XP_011529154.1:p.Glu1619Ter
|
|
XM_011530853.3:c.4843G>T
|
XP_011529155.1:p.Glu1615Ter
|
|
NM_001847.4:c.4876G>T
|
NP_001838.2:p.Glu1626Ter
|
|
NM_033641.4:c.4873G>T
MANE Select
|
NP_378667.1:p.Glu1625Ter
|
|
NM_001287758.2:c.4924G>T
|
NP_001274687.1:p.Glu1642Ter
|
|
NM_001287759.2:c.4801G>T
|
NP_001274688.1:p.Glu1601Ter
|
|
NM_001287760.2:c.4702G>T
|
NP_001274689.1:p.Glu1568Ter
|
|