ENST00000450114.7:c.1449T>A
MANE Select
|
ENSP00000402084.2:p.Leu483=
|
|
ENST00000530712.6:c.267T>A
|
ENSP00000434148.2:p.Leu89=
|
|
ENST00000680141.1:c.*399T>A
|
ENSP00000506686.1:n.*399T>A
|
|
ENST00000681684.1:c.807T>A
|
ENSP00000506667.1:p.Leu269=
|
|
ENST00000299613.10:c.807T>A
|
ENSP00000299613.5:p.Leu269=
|
|
ENST00000450114.6:c.1449T>A
|
ENSP00000402084.2:p.Leu483=
|
|
ENST00000524612.5:c.333T>A
|
ENSP00000434446.1:p.Leu111=
|
|
ENST00000530175.5:c.296T>A
|
|
|
ENST00000530712.5:c.267T>A
|
ENSP00000434148.1:p.Leu89=
|
|
ENST00000532275.1:n.236T>A
|
|
|
NM_001143976.1:c.807T>A
|
NP_001137448.1:p.Leu269=
|
|
NM_003390.3:c.1449T>A
|
NP_003381.1:p.Leu483=
|
|
XM_005253118.3:c.1449T>A
|
XP_005253175.1:p.Leu483=
|
|
XM_005253119.3:c.807T>A
|
XP_005253176.1:p.Leu269=
|
|
NM_003390.4:c.1449T>A
MANE Select
|
NP_003381.1:p.Leu483=
|
|
NM_001143976.2:c.807T>A
|
NP_001137448.1:p.Leu269=
|
|