ENST00000700555.2:n.595G>T
|
|
|
ENST00000700557.2:n.184G>T
|
|
|
ENST00000700559.2:c.2092G>T
|
ENSP00000515065.2:p.Asp698Tyr
|
|
ENST00000546498.2:n.779G>T
|
|
|
ENST00000549461.2:n.631G>T
|
|
|
ENST00000700555.1:c.523G>T
|
ENSP00000515062.1:p.Asp175Tyr
|
|
ENST00000700556.1:c.563G>T
|
|
|
ENST00000700557.1:c.103G>T
|
ENSP00000515064.1:p.Asp35Tyr
|
|
ENST00000700558.1:n.306G>T
|
|
|
ENST00000700559.1:c.1307G>T
|
|
|
ENST00000700560.1:n.1307G>T
|
|
|
ENST00000700561.1:n.1433G>T
|
|
|
ENST00000070846.11:c.2224G>T
|
ENSP00000070846.6:p.Asp742Tyr
|
|
ENST00000340811.9:c.2092G>T
MANE Select
|
ENSP00000342800.5:p.Asp698Tyr
|
|
ENST00000070846.10:c.2224G>T
|
ENSP00000070846.6:p.Asp742Tyr
|
|
ENST00000340811.8:c.2092G>T
|
ENSP00000342800.4:p.Asp698Tyr
|
|
ENST00000549461.1:n.538G>T
|
|
|
ENST00000613243.1:c.2224G>T
|
ENSP00000478295.1:p.Asp742Tyr
|
|
NM_001005242.2:c.2092G>T
|
NP_001005242.2:p.Asp698Tyr
|
|
NM_004572.3:c.2224G>T , LRG_398t1:c.2224G>T
|
NP_004563.2:p.Asp742Tyr
|
|
NM_001005242.3:c.2092G>T
MANE Select
|
NP_001005242.2:p.Asp698Tyr
|
|
NM_004572.4:c.2224G>T
|
NP_004563.2:p.Asp742Tyr
|
|