ENST00000333891.14:c.11172G>A
MANE Select
|
ENSP00000334319.8:p.Leu3724=
|
|
ENST00000333891.13:c.11172G>A
|
ENSP00000334319.8:p.Leu3724=
|
|
ENST00000423517.6:c.11172G>A
|
ENSP00000388393.2:p.Leu3724=
|
|
ENST00000437081.1:c.1332G>A
|
ENSP00000393760.1:p.Leu444=
|
|
NM_014510.2:c.11172G>A
|
NP_055325.2:p.Leu3724=
|
|
NM_033026.5:c.11172G>A
|
NP_149015.2:p.Leu3724=
|
|
XM_017012006.2:c.4077G>A
|
XP_016867495.1:p.Leu1359=
|
|
XM_017012007.1:c.4077G>A
|
XP_016867496.1:p.Leu1359=
|
|
XR_001744643.2:n.12741G>A
|
|
|
NM_033026.6:c.11172G>A
MANE Select
|
NP_149015.2:p.Leu3724=
|
|
NM_014510.3:c.11172G>A
|
NP_055325.2:p.Leu3724=
|
|