ENST00000436117.3:c.*491A>T
|
ENSP00000410980.2:n.*491A>T
|
|
ENST00000318493.11:c.2940A>T
|
ENSP00000317272.6:p.Lys980Asn
|
|
ENST00000397752.8:c.2886A>T
MANE Select
|
ENSP00000380860.3:p.Lys962Asn
|
|
ENST00000318493.10:c.2940A>T
|
ENSP00000317272.6:p.Lys980Asn
|
|
ENST00000397752.7:c.2886A>T
|
ENSP00000380860.3:p.Lys962Asn
|
|
ENST00000454623.1:c.282A>T
|
ENSP00000398140.1:p.Lys94Asn
|
|
NM_000245.2:c.2886A>T
|
NP_000236.2:p.Lys962Asn
|
|
NM_001127500.1:c.2940A>T , LRG_662t1:c.2940A>T
|
NP_001120972.1:p.Lys980Asn
|
|
XM_006715990.2:c.1596A>T
|
XP_006716053.1:p.Lys532Asn
|
|
XM_006715991.2:c.1596A>T
|
XP_006716054.1:p.Lys532Asn
|
|
XM_011516223.1:c.2943A>T
|
XP_011514525.1:p.Lys981Asn
|
|
NM_000245.3:c.2886A>T
|
NP_000236.2:p.Lys962Asn
|
|
NM_001127500.2:c.2940A>T
|
NP_001120972.1:p.Lys980Asn
|
|
NM_001324402.1:c.1596A>T
|
NP_001311331.1:p.Lys532Asn
|
|
XR_001744772.1:n.3017A>T
|
|
|
NM_001127500.3:c.2940A>T
|
NP_001120972.1:p.Lys980Asn
|
|
NM_000245.4:c.2886A>T
MANE Select
|
NP_000236.2:p.Lys962Asn
|
|
NM_001324402.2:c.1596A>T
|
NP_001311331.1:p.Lys532Asn
|
|