ENST00000700555.2:n.162T>A
|
|
|
ENST00000700559.2:c.1650T>A
|
ENSP00000515065.2:p.Ile550=
|
|
ENST00000700563.2:c.1650T>A
|
ENSP00000515066.2:p.Ile550=
|
|
ENST00000546498.2:n.337T>A
|
|
|
ENST00000700555.1:c.90T>A
|
ENSP00000515062.1:p.Ile30=
|
|
ENST00000700556.1:c.121T>A
|
|
|
ENST00000700559.1:c.865T>A
|
|
|
ENST00000700560.1:n.865T>A
|
|
|
ENST00000700561.1:n.991T>A
|
|
|
ENST00000700563.1:c.1604T>A
|
|
|
ENST00000700564.1:n.1654T>A
|
|
|
ENST00000070846.11:c.1782T>A
|
ENSP00000070846.6:p.Ile594=
|
|
ENST00000340811.9:c.1650T>A
MANE Select
|
ENSP00000342800.5:p.Ile550=
|
|
ENST00000070846.10:c.1782T>A
|
ENSP00000070846.6:p.Ile594=
|
|
ENST00000340811.8:c.1650T>A
|
ENSP00000342800.4:p.Ile550=
|
|
ENST00000546498.1:n.337T>A
|
|
|
ENST00000552612.5:n.71T>A
|
|
|
ENST00000613243.1:c.1782T>A
|
ENSP00000478295.1:p.Ile594=
|
|
NM_001005242.2:c.1650T>A
|
NP_001005242.2:p.Ile550=
|
|
NM_004572.3:c.1782T>A , LRG_398t1:c.1782T>A
|
NP_004563.2:p.Ile594=
|
|
NM_001005242.3:c.1650T>A
MANE Select
|
NP_001005242.2:p.Ile550=
|
|
NM_004572.4:c.1782T>A
|
NP_004563.2:p.Ile594=
|
|