ENST00000700555.2:n.983G>A
|
|
|
ENST00000700557.2:n.572G>A
|
|
|
ENST00000700559.2:c.2290G>A
|
ENSP00000515065.2:p.Gly764Arg
|
|
ENST00000546498.2:n.1167G>A
|
|
|
ENST00000549461.2:n.972G>A
|
|
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ENST00000700555.1:c.911G>A
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ENSP00000515062.1:p.Arg304Gln
|
|
ENST00000700556.1:c.951G>A
|
|
|
ENST00000700557.1:c.491G>A
|
ENSP00000515064.1:p.Arg164Gln
|
|
ENST00000700558.1:n.694G>A
|
|
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ENST00000700559.1:c.1505G>A
|
|
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ENST00000700560.1:n.1846G>A
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|
|
ENST00000070846.11:c.2612G>A
|
ENSP00000070846.6:p.Arg871Gln
|
|
ENST00000340811.9:c.2480G>A
MANE Select
|
ENSP00000342800.5:p.Arg827Gln
|
|
ENST00000070846.10:c.2612G>A
|
ENSP00000070846.6:p.Arg871Gln
|
|
ENST00000340811.8:c.2480G>A
|
ENSP00000342800.4:p.Arg827Gln
|
|
ENST00000546769.1:n.267G>A
|
|
|
ENST00000613243.1:c.2610G>A
|
ENSP00000478295.1:n.2610G>A
|
|
NM_001005242.2:c.2480G>A
|
NP_001005242.2:p.Arg827Gln
|
|
NM_004572.3:c.2612G>A , LRG_398t1:c.2612G>A
|
NP_004563.2:p.Arg871Gln
|
|
NM_001005242.3:c.2480G>A
MANE Select
|
NP_001005242.2:p.Arg827Gln
|
|
NM_004572.4:c.2612G>A
|
NP_004563.2:p.Arg871Gln
|
|