ENST00000436117.3:c.*1391C=
|
ENSP00000410980.2:n.*1391C=
|
|
ENST00000318493.11:c.3840C=
|
ENSP00000317272.6:p.Thr1280=
|
|
ENST00000397752.8:c.3786C=
MANE Select
|
ENSP00000380860.3:p.Thr1262=
|
|
ENST00000318493.10:c.3840C=
|
ENSP00000317272.6:p.Thr1280=
|
|
ENST00000397752.7:c.3786C=
|
ENSP00000380860.3:p.Thr1262=
|
|
NM_000245.2:c.3786C=
|
NP_000236.2:p.Thr1262=
|
|
NM_001127500.1:c.3840C= , LRG_662t1:c.3840C=
|
NP_001120972.1:p.Thr1280=
|
|
XM_006715990.2:c.2496C=
|
XP_006716053.1:p.Thr832=
|
|
XM_006715991.2:c.2496C=
|
XP_006716054.1:p.Thr832=
|
|
XM_011516223.1:c.3843C=
|
XP_011514525.1:p.Thr1281=
|
|
NM_000245.3:c.3786C=
|
NP_000236.2:p.Thr1262=
|
|
NM_001127500.2:c.3840C=
|
NP_001120972.1:p.Thr1280=
|
|
NM_001324402.1:c.2496C=
|
NP_001311331.1:p.Thr832=
|
|
XR_001744772.1:n.3917C=
|
|
|
NM_001127500.3:c.3840C=
|
NP_001120972.1:p.Thr1280=
|
|
NM_000245.4:c.3786C=
MANE Select
|
NP_000236.2:p.Thr1262=
|
|
NM_001324402.2:c.2496C=
|
NP_001311331.1:p.Thr832=
|
|