ENST00000436117.3:c.*1256A=
|
ENSP00000410980.2:n.*1256A=
|
|
ENST00000318493.11:c.3705A=
|
ENSP00000317272.6:p.Thr1235=
|
|
ENST00000397752.8:c.3651A=
MANE Select
|
ENSP00000380860.3:p.Thr1217=
|
|
ENST00000318493.10:c.3705A=
|
ENSP00000317272.6:p.Thr1235=
|
|
ENST00000397752.7:c.3651A=
|
ENSP00000380860.3:p.Thr1217=
|
|
NM_000245.2:c.3651A=
|
NP_000236.2:p.Thr1217=
|
|
NM_001127500.1:c.3705A= , LRG_662t1:c.3705A=
|
NP_001120972.1:p.Thr1235=
|
|
XM_006715990.2:c.2361A=
|
XP_006716053.1:p.Thr787=
|
|
XM_006715991.2:c.2361A=
|
XP_006716054.1:p.Thr787=
|
|
XM_011516223.1:c.3708A=
|
XP_011514525.1:p.Thr1236=
|
|
NM_000245.3:c.3651A=
|
NP_000236.2:p.Thr1217=
|
|
NM_001127500.2:c.3705A=
|
NP_001120972.1:p.Thr1235=
|
|
NM_001324402.1:c.2361A=
|
NP_001311331.1:p.Thr787=
|
|
XR_001744772.1:n.3782A=
|
|
|
NM_001127500.3:c.3705A=
|
NP_001120972.1:p.Thr1235=
|
|
NM_000245.4:c.3651A=
MANE Select
|
NP_000236.2:p.Thr1217=
|
|
NM_001324402.2:c.2361A=
|
NP_001311331.1:p.Thr787=
|
|