ENST00000367408.6:n.3334T>C
|
|
|
ENST00000367409.9:c.10047T>C
MANE Select
|
ENSP00000356379.4:p.Leu3349=
|
|
ENST00000680265.1:c.10269T>C
|
ENSP00000505384.1:p.Leu3423=
|
|
ENST00000680710.1:c.10023T>C
|
ENSP00000506676.1:p.Leu3341=
|
|
ENST00000294732.11:c.5292T>C
|
ENSP00000294732.7:p.Leu1764=
|
|
ENST00000367408.5:c.3042T>C
|
ENSP00000356378.1:p.Leu1014=
|
|
ENST00000367409.8:c.10047T>C
|
ENSP00000356379.4:p.Leu3349=
|
|
ENST00000612785.1:c.4005T>C
|
ENSP00000479244.1:p.Leu1335=
|
|
NM_001206846.1:c.5292T>C
|
NP_001193775.1:p.Leu1764=
|
|
NM_018136.4:c.10047T>C
|
NP_060606.3:p.Leu3349=
|
|
NM_018136.5:c.10047T>C
MANE Select
|
NP_060606.3:p.Leu3349=
|
|
NM_001206846.2:c.5292T>C
|
NP_001193775.1:p.Leu1764=
|
|