ENST00000436117.3:c.*470G=
|
ENSP00000410980.2:n.*470G=
|
|
ENST00000318493.11:c.2919G=
|
ENSP00000317272.6:p.Leu973=
|
|
ENST00000397752.8:c.2865G=
MANE Select
|
ENSP00000380860.3:p.Leu955=
|
|
ENST00000318493.10:c.2919G=
|
ENSP00000317272.6:p.Leu973=
|
|
ENST00000397752.7:c.2865G=
|
ENSP00000380860.3:p.Leu955=
|
|
ENST00000454623.1:c.261G=
|
ENSP00000398140.1:p.Leu87=
|
|
NM_000245.2:c.2865G=
|
NP_000236.2:p.Leu955=
|
|
NM_001127500.1:c.2919G= , LRG_662t1:c.2919G=
|
NP_001120972.1:p.Leu973=
|
|
XM_006715990.2:c.1575G=
|
XP_006716053.1:p.Leu525=
|
|
XM_006715991.2:c.1575G=
|
XP_006716054.1:p.Leu525=
|
|
XM_011516223.1:c.2922G=
|
XP_011514525.1:p.Leu974=
|
|
NM_000245.3:c.2865G=
|
NP_000236.2:p.Leu955=
|
|
NM_001127500.2:c.2919G=
|
NP_001120972.1:p.Leu973=
|
|
NM_001324402.1:c.1575G=
|
NP_001311331.1:p.Leu525=
|
|
XR_001744772.1:n.2996G=
|
|
|
NM_001127500.3:c.2919G=
|
NP_001120972.1:p.Leu973=
|
|
NM_000245.4:c.2865G=
MANE Select
|
NP_000236.2:p.Leu955=
|
|
NM_001324402.2:c.1575G=
|
NP_001311331.1:p.Leu525=
|
|