ENST00000375708.4:c.678C>T
MANE Select
|
ENSP00000364860.3:p.Phe226=
|
|
ENST00000375708.3:c.678C>T
|
ENSP00000364860.3:p.Phe226=
|
|
ENST00000375715.5:c.258C>T
|
ENSP00000364867.1:p.Phe86=
|
|
ENST00000550066.5:n.1146C>T
|
|
|
NM_004560.3:c.678C>T
|
NP_004551.2:p.Phe226=
|
|
XM_005252008.3:c.258C>T
|
XP_005252065.1:p.Phe86=
|
|
XM_006717121.2:c.258C>T
|
XP_006717184.1:p.Phe86=
|
|
XM_011518721.1:c.258C>T
|
XP_011517023.1:p.Phe86=
|
|
NM_001318204.1:c.678C>T
|
NP_001305133.1:p.Phe226=
|
|
XM_005252008.4:c.258C>T
|
XP_005252065.1:p.Phe86=
|
|
XM_006717121.3:c.258C>T
|
XP_006717184.1:p.Phe86=
|
|
XM_017014762.1:c.669C>T
|
XP_016870251.1:p.Phe223=
|
|
XM_017014763.1:c.258C>T
|
XP_016870252.1:p.Phe86=
|
|
XR_001746315.1:n.921C>T
|
|
|
NM_004560.4:c.678C>T
MANE Select
|
NP_004551.2:p.Phe226=
|
|
NM_001318204.2:c.678C>T
|
NP_001305133.1:p.Phe226=
|
|