ENST00000700555.2:n.408T>G
|
|
|
ENST00000700559.2:c.1905T>G
|
ENSP00000515065.2:p.His635Gln
|
|
ENST00000700563.2:c.1905T>G
|
ENSP00000515066.2:p.His635Gln
|
|
ENST00000546498.2:n.592T>G
|
|
|
ENST00000549461.2:n.444T>G
|
|
|
ENST00000700555.1:c.336T>G
|
ENSP00000515062.1:p.His112Gln
|
|
ENST00000700556.1:c.376T>G
|
|
|
ENST00000700558.1:n.119T>G
|
|
|
ENST00000700559.1:c.1120T>G
|
|
|
ENST00000700560.1:n.1120T>G
|
|
|
ENST00000700561.1:n.1246T>G
|
|
|
ENST00000700562.1:n.443T>G
|
|
|
ENST00000700563.1:c.1859T>G
|
|
|
ENST00000700564.1:n.1909T>G
|
|
|
ENST00000070846.11:c.2037T>G
|
ENSP00000070846.6:p.His679Gln
|
|
ENST00000340811.9:c.1905T>G
MANE Select
|
ENSP00000342800.5:p.His635Gln
|
|
ENST00000070846.10:c.2037T>G
|
ENSP00000070846.6:p.His679Gln
|
|
ENST00000340811.8:c.1905T>G
|
ENSP00000342800.4:p.His635Gln
|
|
ENST00000549461.1:n.351T>G
|
|
|
ENST00000552612.5:n.326T>G
|
|
|
ENST00000613243.1:c.2037T>G
|
ENSP00000478295.1:p.His679Gln
|
|
NM_001005242.2:c.1905T>G
|
NP_001005242.2:p.His635Gln
|
|
NM_004572.3:c.2037T>G , LRG_398t1:c.2037T>G
|
NP_004563.2:p.His679Gln
|
|
NM_001005242.3:c.1905T>G
MANE Select
|
NP_001005242.2:p.His635Gln
|
|
NM_004572.4:c.2037T>G
|
NP_004563.2:p.His679Gln
|
|