ENST00000700555.2:n.840G>T
|
|
|
ENST00000700557.2:n.429G>T
|
|
|
ENST00000700559.2:c.2168-3398G>T
|
ENSP00000515065.2:n.2168-3398G>T
|
|
ENST00000546498.2:n.1024G>T
|
|
|
ENST00000549461.2:n.829G>T
|
|
|
ENST00000700555.1:c.768G>T
|
ENSP00000515062.1:p.Met256Ile
|
|
ENST00000700556.1:c.808G>T
|
|
|
ENST00000700557.1:c.348G>T
|
ENSP00000515064.1:p.Met116Ile
|
|
ENST00000700558.1:n.551G>T
|
|
|
ENST00000700559.1:c.1383-3398G>T
|
|
|
ENST00000700560.1:n.1552G>T
|
|
|
ENST00000700561.1:n.1678G>T
|
|
|
ENST00000070846.11:c.2469G>T
|
ENSP00000070846.6:p.Met823Ile
|
|
ENST00000340811.9:c.2337G>T
MANE Select
|
ENSP00000342800.5:p.Met779Ile
|
|
ENST00000070846.10:c.2469G>T
|
ENSP00000070846.6:p.Met823Ile
|
|
ENST00000340811.8:c.2337G>T
|
ENSP00000342800.4:p.Met779Ile
|
|
ENST00000613243.1:c.2467G>T
|
ENSP00000478295.1:p.Gly823Cys
|
|
NM_001005242.2:c.2337G>T
|
NP_001005242.2:p.Met779Ile
|
|
NM_004572.3:c.2469G>T , LRG_398t1:c.2469G>T
|
NP_004563.2:p.Met823Ile
|
|
NM_001005242.3:c.2337G>T
MANE Select
|
NP_001005242.2:p.Met779Ile
|
|
NM_004572.4:c.2469G>T
|
NP_004563.2:p.Met823Ile
|
|