ENST00000700555.2:n.517A>G
|
|
|
ENST00000700557.2:n.106A>G
|
|
|
ENST00000700559.2:c.2014A>G
|
ENSP00000515065.2:p.Met672Val
|
|
ENST00000546498.2:n.701A>G
|
|
|
ENST00000549461.2:n.553A>G
|
|
|
ENST00000700555.1:c.445A>G
|
ENSP00000515062.1:p.Met149Val
|
|
ENST00000700556.1:c.485A>G
|
|
|
ENST00000700557.1:c.25A>G
|
ENSP00000515064.1:p.Met9Val
|
|
ENST00000700558.1:n.228A>G
|
|
|
ENST00000700559.1:c.1229A>G
|
|
|
ENST00000700560.1:n.1229A>G
|
|
|
ENST00000700561.1:n.1355A>G
|
|
|
ENST00000070846.11:c.2146A>G
|
ENSP00000070846.6:p.Met716Val
|
|
ENST00000340811.9:c.2014A>G
MANE Select
|
ENSP00000342800.5:p.Met672Val
|
|
ENST00000070846.10:c.2146A>G
|
ENSP00000070846.6:p.Met716Val
|
|
ENST00000340811.8:c.2014A>G
|
ENSP00000342800.4:p.Met672Val
|
|
ENST00000549461.1:n.460A>G
|
|
|
ENST00000613243.1:c.2146A>G
|
ENSP00000478295.1:p.Met716Val
|
|
NM_001005242.2:c.2014A>G
|
NP_001005242.2:p.Met672Val
|
|
NM_004572.3:c.2146A>G , LRG_398t1:c.2146A>G
|
NP_004563.2:p.Met716Val
|
|
NM_001005242.3:c.2014A>G
MANE Select
|
NP_001005242.2:p.Met672Val
|
|
NM_004572.4:c.2146A>G
|
NP_004563.2:p.Met716Val
|
|