ENST00000367698.4:c.1105G>T
MANE Select
|
ENSP00000356671.3:p.Asp369Tyr
|
|
ENST00000367698.3:c.1105G>T
|
ENSP00000356671.3:p.Asp369Tyr
|
|
ENST00000617423.4:c.560-2107G>T
|
ENSP00000478688.1:n.560-2107G>T
|
|
NM_000488.3:c.1105G>T , LRG_577t1:c.1105G>T
|
NP_000479.1:p.Asp369Tyr
|
|
XM_005245198.2:c.961G>T
|
XP_005245255.1:p.Asp321Tyr
|
|
NM_001365052.1:c.961G>T
|
NP_001351981.1:p.Asp321Tyr
|
|
NM_000488.4:c.1105G>T
MANE Select
|
NP_000479.1:p.Asp369Tyr
|
|
NM_001365052.2:c.961G>T
|
NP_001351981.1:p.Asp321Tyr
|
|
NM_001386302.1:c.1228G>T
|
NP_001373231.1:p.Asp410Tyr
|
|
NM_001386303.1:c.1186G>T
|
NP_001373232.1:p.Asp396Tyr
|
|
NM_001386304.1:c.1084G>T
|
NP_001373233.1:p.Asp362Tyr
|
|
NM_001386305.1:c.1048G>T
|
NP_001373234.1:p.Asp350Tyr
|
|
NM_001386306.1:c.889G>T
|
NP_001373235.1:p.Asp297Tyr
|
|