ENST00000700555.2:n.448A=
|
|
|
ENST00000700559.2:c.1945A=
|
ENSP00000515065.2:p.Ser649=
|
|
ENST00000700563.2:c.1945A=
|
ENSP00000515066.2:p.Ser649=
|
|
ENST00000546498.2:n.632A=
|
|
|
ENST00000549461.2:n.484A=
|
|
|
ENST00000700555.1:c.376A=
|
ENSP00000515062.1:p.Ser126=
|
|
ENST00000700556.1:c.416A=
|
|
|
ENST00000700558.1:n.159A=
|
|
|
ENST00000700559.1:c.1160A=
|
|
|
ENST00000700560.1:n.1160A=
|
|
|
ENST00000700561.1:n.1286A=
|
|
|
ENST00000700562.1:n.483A=
|
|
|
ENST00000700563.1:c.1899A=
|
|
|
ENST00000700564.1:n.1949A=
|
|
|
ENST00000070846.11:c.2077A=
|
ENSP00000070846.6:p.Ser693=
|
|
ENST00000340811.9:c.1945A=
MANE Select
|
ENSP00000342800.5:p.Ser649=
|
|
ENST00000070846.10:c.2077A=
|
ENSP00000070846.6:p.Ser693=
|
|
ENST00000340811.8:c.1945A=
|
ENSP00000342800.4:p.Ser649=
|
|
ENST00000549461.1:n.391A=
|
|
|
ENST00000552612.5:n.366A=
|
|
|
ENST00000613243.1:c.2077A=
|
ENSP00000478295.1:p.Ser693=
|
|
NM_001005242.2:c.1945A=
|
NP_001005242.2:p.Ser649=
|
|
NM_004572.3:c.2077A= , LRG_398t1:c.2077A=
|
NP_004563.2:p.Ser693=
|
|
NM_001005242.3:c.1945A=
MANE Select
|
NP_001005242.2:p.Ser649=
|
|
NM_004572.4:c.2077A=
|
NP_004563.2:p.Ser693=
|
|