|
ENST00000698508.1:c.1679G>A
|
ENSP00000513759.1:p.Cys560Tyr
|
|
|
ENST00000698509.1:n.1819G>A
|
|
|
|
ENST00000264972.10:c.1679G>A
MANE Select
|
ENSP00000264972.5:p.Cys560Tyr
|
|
|
ENST00000264972.9:c.1679G>A
|
ENSP00000264972.5:p.Cys560Tyr
|
|
|
ENST00000451498.2:c.758G>A
|
ENSP00000400475.2:p.Cys253Tyr
|
|
|
ENST00000463643.5:n.1540G>A
|
|
|
|
ENST00000487283.5:n.2731G>A
|
|
|
|
ENST00000489250.1:n.132G>A
|
|
|
|
NM_001079.3:c.1679G>A , LRG_126t1:c.1679G>A
|
NP_001070.2:p.Cys560Tyr
|
|
|
NM_207519.1:c.758G>A
|
NP_997402.1:p.Cys253Tyr
|
|
|
XM_005264015.3:c.1661G>A
|
XP_005264072.1:p.Cys554Tyr
|
|
|
XM_006712728.2:c.1679G>A
|
XP_006712791.1:p.Cys560Tyr
|
|
|
XM_011511783.1:c.1679G>A
|
XP_011510085.1:p.Cys560Tyr
|
|
|
XR_923018.1:n.1881G>A
|
|
|
|
XR_923019.1:n.1881G>A
|
|
|
|
XR_923020.1:n.1881G>A
|
|
|
|
XM_017004867.1:c.2048G>A
|
XP_016860356.1:p.Cys683Tyr
|
|
|
XM_017004868.1:c.2030G>A
|
XP_016860357.1:p.Cys677Tyr
|
|
|
XM_017004869.1:c.2048G>A
|
XP_016860358.1:p.Cys683Tyr
|
|
|
XM_017004870.1:c.2048G>A
|
XP_016860359.1:p.Cys683Tyr
|
|
|
XR_001738925.1:n.3287G>A
|
|
|
|
XR_001738926.1:n.3287G>A
|
|
|
|
XR_001738927.1:n.3287G>A
|
|
|
|
NM_001079.4:c.1679G>A
MANE Select
|
NP_001070.2:p.Cys560Tyr
|
|
|
NM_001378594.1:c.1679G>A
|
NP_001365523.1:p.Cys560Tyr
|
|
|
NM_207519.2:c.758G>A
|
NP_997402.1:p.Cys253Tyr
|
|
