ENST00000644991.3:c.716G>T
MANE Select
|
ENSP00000495607.1:p.Arg239Ile
|
|
ENST00000614701.4:c.716G>T
|
ENSP00000482885.1:p.Arg239Ile
|
|
ENST00000616559.4:c.842G>T
|
ENSP00000483259.1:p.Arg281Ile
|
|
NM_001145026.1:c.716G>T
|
NP_001138498.1:p.Arg239Ile
|
|
XM_011538290.1:c.716G>T
|
XP_011536592.1:p.Arg239Ile
|
|
XM_017019273.1:c.1382G>T
|
XP_016874762.1:p.Arg461Ile
|
|
XM_017019274.1:c.1382G>T
|
XP_016874763.1:p.Arg461Ile
|
|
XM_017019275.1:c.1382G>T
|
XP_016874764.1:p.Arg461Ile
|
|
XR_001748688.1:n.1519G>T
|
|
|
XR_001748689.1:n.1519G>T
|
|
|
NM_001145026.2:c.716G>T
MANE Select
|
NP_001138498.1:p.Arg239Ile
|
|