ENST00000266771.10:c.592T>A
MANE Select
|
ENSP00000266771.5:p.Phe198Ile
|
|
ENST00000266771.9:c.592T>A
|
ENSP00000266771.5:p.Phe198Ile
|
|
ENST00000366292.6:n.904T>A
|
|
|
ENST00000376740.8:c.171T>A
|
|
|
ENST00000376744.8:c.428T>A
|
|
|
ENST00000535272.1:n.386T>A
|
|
|
ENST00000539703.1:n.242T>A
|
|
|
NM_145648.3:c.592T>A
|
NP_663623.1:p.Phe198Ile
|
|
XM_011537895.1:c.742T>A
|
XP_011536197.1:p.Phe248Ile
|
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XR_429081.2:n.615T>A
|
|
|
XR_944494.1:n.765T>A
|
|
|
XR_944495.1:n.765T>A
|
|
|
XR_944496.1:n.765T>A
|
|
|
XR_944497.1:n.765T>A
|
|
|
XM_017018791.1:c.742T>A
|
XP_016874280.1:p.Phe248Ile
|
|
XM_017018792.1:c.742T>A
|
XP_016874281.1:p.Phe248Ile
|
|
XM_017018793.1:c.592T>A
|
XP_016874282.1:p.Phe198Ile
|
|
XR_002957287.1:n.615T>A
|
|
|
XR_944496.2:n.765T>A
|
|
|
NM_145648.4:c.592T>A
MANE Select
|
NP_663623.1:p.Phe198Ile
|
|