ENST00000700555.2:n.560G>A
|
|
|
ENST00000700557.2:n.149G>A
|
|
|
ENST00000700559.2:c.2057G>A
|
ENSP00000515065.2:p.Gly686Asp
|
|
ENST00000546498.2:n.744G>A
|
|
|
ENST00000549461.2:n.596G>A
|
|
|
ENST00000700555.1:c.488G>A
|
ENSP00000515062.1:p.Gly163Asp
|
|
ENST00000700556.1:c.528G>A
|
|
|
ENST00000700557.1:c.68G>A
|
ENSP00000515064.1:p.Gly23Asp
|
|
ENST00000700558.1:n.271G>A
|
|
|
ENST00000700559.1:c.1272G>A
|
|
|
ENST00000700560.1:n.1272G>A
|
|
|
ENST00000700561.1:n.1398G>A
|
|
|
ENST00000070846.11:c.2189G>A
|
ENSP00000070846.6:p.Gly730Asp
|
|
ENST00000340811.9:c.2057G>A
MANE Select
|
ENSP00000342800.5:p.Gly686Asp
|
|
ENST00000070846.10:c.2189G>A
|
ENSP00000070846.6:p.Gly730Asp
|
|
ENST00000340811.8:c.2057G>A
|
ENSP00000342800.4:p.Gly686Asp
|
|
ENST00000549461.1:n.503G>A
|
|
|
ENST00000613243.1:c.2189G>A
|
ENSP00000478295.1:p.Gly730Asp
|
|
NM_001005242.2:c.2057G>A
|
NP_001005242.2:p.Gly686Asp
|
|
NM_004572.3:c.2189G>A , LRG_398t1:c.2189G>A
|
NP_004563.2:p.Gly730Asp
|
|
NM_001005242.3:c.2057G>A
MANE Select
|
NP_001005242.2:p.Gly686Asp
|
|
NM_004572.4:c.2189G>A
|
NP_004563.2:p.Gly730Asp
|
|