ENST00000372600.9:c.51C>T
MANE Select
|
ENSP00000361682.4:p.Tyr17=
|
|
ENST00000259324.5:c.51C>T
|
ENSP00000259324.5:p.Tyr17=
|
|
ENST00000372599.7:c.51C>T
|
ENSP00000361680.3:p.Tyr17=
|
|
ENST00000372600.8:c.51C>T
|
ENSP00000361682.4:p.Tyr17=
|
|
NM_001127244.1:c.51C>T
|
NP_001120716.1:p.Tyr17=
|
|
NM_001127245.1:c.51C>T
|
NP_001120717.1:p.Tyr17=
|
|
NM_019594.3:c.51C>T , LRG_80t1:c.51C>T
|
NP_062540.2:p.Tyr17=
|
|
XM_005252095.2:c.51C>T
|
XP_005252152.1:p.Tyr17=
|
|
XM_005252096.2:c.51C>T
|
XP_005252153.1:p.Tyr17=
|
|
XM_006717186.2:c.51C>T
|
XP_006717249.1:p.Tyr17=
|
|
XM_011518863.1:c.51C>T
|
XP_011517165.1:p.Tyr17=
|
|
XM_011518864.1:c.51C>T
|
XP_011517166.1:p.Tyr17=
|
|
XM_011518865.1:c.51C>T
|
XP_011517167.1:p.Tyr17=
|
|
XM_005252096.4:c.51C>T
|
XP_005252153.1:p.Tyr17=
|
|
XM_011518864.2:c.51C>T
|
XP_011517166.1:p.Tyr17=
|
|
XM_011518865.2:c.51C>T
|
XP_011517167.1:p.Tyr17=
|
|
NM_001127245.2:c.51C>T
|
NP_001120717.1:p.Tyr17=
|
|
NM_001127244.2:c.51C>T
|
NP_001120716.1:p.Tyr17=
|
|
NM_019594.4:c.51C>T
MANE Select
|
NP_062540.2:p.Tyr17=
|
|