ENST00000367408.6:n.3337G=
|
|
|
ENST00000367409.9:c.10050G=
MANE Select
|
ENSP00000356379.4:p.Leu3350=
|
|
ENST00000680265.1:c.10272G=
|
ENSP00000505384.1:p.Leu3424=
|
|
ENST00000680710.1:c.10026G=
|
ENSP00000506676.1:p.Leu3342=
|
|
ENST00000294732.11:c.5295G=
|
ENSP00000294732.7:p.Leu1765=
|
|
ENST00000367408.5:c.3045G=
|
ENSP00000356378.1:p.Leu1015=
|
|
ENST00000367409.8:c.10050G=
|
ENSP00000356379.4:p.Leu3350=
|
|
ENST00000612785.1:c.4008G=
|
ENSP00000479244.1:p.Leu1336=
|
|
NM_001206846.1:c.5295G=
|
NP_001193775.1:p.Leu1765=
|
|
NM_018136.4:c.10050G=
|
NP_060606.3:p.Leu3350=
|
|
NM_018136.5:c.10050G=
MANE Select
|
NP_060606.3:p.Leu3350=
|
|
NM_001206846.2:c.5295G=
|
NP_001193775.1:p.Leu1765=
|
|