ENST00000367099.4:n.1492A>G
|
|
|
ENST00000471071.2:c.232A>G
|
ENSP00000493073.2:p.Ile78Val
|
|
ENST00000640756.2:n.297A>G
|
|
|
ENST00000659065.2:c.370A>G
|
ENSP00000499588.1:p.Ile124Val
|
|
ENST00000659642.2:c.370A>G
|
ENSP00000499509.1:p.Ile124Val
|
|
ENST00000664374.2:c.370A>G
|
ENSP00000499664.1:p.Ile124Val
|
|
ENST00000640756.1:n.286A>G
|
|
|
ENST00000659065.1:c.370A>G
|
ENSP00000499588.1:p.Ile124Val
|
|
ENST00000659642.1:c.370A>G
|
ENSP00000499509.1:p.Ile124Val
|
|
ENST00000664374.1:c.370A>G
|
ENSP00000499664.1:p.Ile124Val
|
|
ENST00000423557.1:c.487A>G
MANE Select
|
ENSP00000412237.1:p.Ile163Val
|
|
NM_000572.2:c.487A>G
|
NP_000563.1:p.Ile163Val
|
|
XM_011509506.1:c.487A>G
|
XP_011507808.1:p.Ile163Val
|
|
NM_000572.3:c.487A>G
MANE Select
|
NP_000563.1:p.Ile163Val
|
|
NM_001382624.1:c.232A>G
|
NP_001369553.1:p.Ile78Val
|
|
NR_168466.1:n.784A>G
|
|
|
NR_168467.1:n.314A>G
|
|
|