ENST00000218099.7:c.585T>G
MANE Select
|
ENSP00000218099.2:p.Val195=
|
|
ENST00000643157.1:n.1252T>G
|
|
|
ENST00000218099.6:c.585T>G
|
ENSP00000218099.2:p.Val195=
|
|
ENST00000394090.2:c.471T>G
|
ENSP00000377650.2:p.Val157=
|
|
NM_000133.3:c.585T>G , LRG_556t1:c.585T>G
|
NP_000124.1:p.Val195=
|
|
NM_001313913.1:c.471T>G
|
NP_001300842.1:p.Val157=
|
|
XM_005262397.3:c.456T>G
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XP_005262454.1:p.Val152=
|
|
XM_005262397.4:c.456T>G
|
XP_005262454.1:p.Val152=
|
|
NM_000133.4:c.585T>G
MANE Select
|
NP_000124.1:p.Val195=
|
|
NM_001313913.2:c.471T>G
|
NP_001300842.1:p.Val157=
|
|