ENST00000422097.2:c.2345C>T
|
ENSP00000398776.2:p.Ala782Val
|
|
ENST00000436117.3:c.2264+851C>T
|
ENSP00000410980.2:n.2264+851C>T
|
|
ENST00000318493.11:c.2399C>T
|
ENSP00000317272.6:p.Ala800Val
|
|
ENST00000397752.8:c.2345C>T
MANE Select
|
ENSP00000380860.3:p.Ala782Val
|
|
ENST00000318493.10:c.2399C>T
|
ENSP00000317272.6:p.Ala800Val
|
|
ENST00000397752.7:c.2345C>T
|
ENSP00000380860.3:p.Ala782Val
|
|
ENST00000422097.1:c.185C>T
|
ENSP00000398776.1:p.Ala62Val
|
|
ENST00000436117.2:c.2264+851C>T
|
ENSP00000410980.2:n.2264+851C>T
|
|
NM_000245.2:c.2345C>T
|
NP_000236.2:p.Ala782Val
|
|
NM_001127500.1:c.2399C>T , LRG_662t1:c.2399C>T
|
NP_001120972.1:p.Ala800Val
|
|
XM_006715990.2:c.1055C>T
|
XP_006716053.1:p.Ala352Val
|
|
XM_006715991.2:c.1055C>T
|
XP_006716054.1:p.Ala352Val
|
|
XM_011516223.1:c.2402C>T
|
XP_011514525.1:p.Ala801Val
|
|
NM_000245.3:c.2345C>T
|
NP_000236.2:p.Ala782Val
|
|
NM_001127500.2:c.2399C>T
|
NP_001120972.1:p.Ala800Val
|
|
NM_001324401.1:c.2345C>T
|
NP_001311330.1:p.Ala782Val
|
|
NM_001324402.1:c.1055C>T
|
NP_001311331.1:p.Ala352Val
|
|
XR_001744772.1:n.2495+851C>T
|
|
|
NM_001127500.3:c.2399C>T
|
NP_001120972.1:p.Ala800Val
|
|
NM_000245.4:c.2345C>T
MANE Select
|
NP_000236.2:p.Ala782Val
|
|
NM_001324401.2:c.2345C>T
|
NP_001311330.1:p.Ala782Val
|
|
NM_001324402.2:c.1055C>T
|
NP_001311331.1:p.Ala352Val
|
|
NM_001324401.3:c.2345C>T
|
NP_001311330.1:p.Ala782Val
|
|