ENST00000266771.10:c.561T>A
MANE Select
|
ENSP00000266771.5:p.Gly187=
|
|
ENST00000266771.9:c.561T>A
|
ENSP00000266771.5:p.Gly187=
|
|
ENST00000366292.6:n.873T>A
|
|
|
ENST00000376740.8:c.140T>A
|
|
|
ENST00000376744.8:c.397T>A
|
|
|
ENST00000535272.1:n.355T>A
|
|
|
ENST00000539703.1:n.211T>A
|
|
|
NM_145648.3:c.561T>A
|
NP_663623.1:p.Gly187=
|
|
XM_011537895.1:c.711T>A
|
XP_011536197.1:p.Gly237=
|
|
XR_429081.2:n.584T>A
|
|
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XR_944494.1:n.734T>A
|
|
|
XR_944495.1:n.734T>A
|
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XR_944496.1:n.734T>A
|
|
|
XR_944497.1:n.734T>A
|
|
|
XM_017018791.1:c.711T>A
|
XP_016874280.1:p.Gly237=
|
|
XM_017018792.1:c.711T>A
|
XP_016874281.1:p.Gly237=
|
|
XM_017018793.1:c.561T>A
|
XP_016874282.1:p.Gly187=
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|
XR_002957287.1:n.584T>A
|
|
|
XR_944496.2:n.734T>A
|
|
|
NM_145648.4:c.561T>A
MANE Select
|
NP_663623.1:p.Gly187=
|
|