ENST00000299506.3:c.80T>A
MANE Select
|
ENSP00000299506.3:p.Leu27His
|
|
ENST00000299506.2:c.80T>A
|
ENSP00000299506.2:p.Leu27His
|
|
ENST00000305253.8:c.245T>A
|
ENSP00000305426.4:p.Leu82His
|
|
ENST00000534099.5:c.98T>A
|
ENSP00000434400.1:p.Leu33His
|
|
NM_003320.4:c.245T>A
|
NP_003311.2:p.Leu82His
|
|
NM_177972.2:c.80T>A
|
NP_813977.1:p.Leu27His
|
|
XM_005253109.2:c.206T>A
|
XP_005253166.1:p.Leu69His
|
|
XM_011520344.1:c.116T>A
|
XP_011518646.1:p.Leu39His
|
|
XM_005253109.3:c.206T>A
|
XP_005253166.1:p.Leu69His
|
|
XM_011520344.2:c.116T>A
|
XP_011518646.1:p.Leu39His
|
|
NM_177972.3:c.80T>A
MANE Select
|
NP_813977.1:p.Leu27His
|
|
NM_003320.5:c.245T>A
|
NP_003311.2:p.Leu82His
|
|