ENST00000023064.9:c.782C>T
MANE Select
|
ENSP00000023064.3:p.Pro261Leu
|
|
ENST00000023064.8:c.782C>T
|
ENSP00000023064.3:p.Pro261Leu
|
|
ENST00000587772.1:c.782C>T
|
ENSP00000468439.1:p.Pro261Leu
|
|
ENST00000589659.1:n.727C>T
|
|
|
ENST00000590341.5:c.782C>T
|
ENSP00000464822.1:p.Pro261Leu
|
|
ENST00000590465.5:c.*929C>T
|
ENSP00000468076.1:n.*929C>T
|
|
ENST00000592232.5:c.*288C>T
|
ENSP00000465563.1:n.*288C>T
|
|
NM_001126335.1:c.782C>T
|
NP_001119807.1:p.Pro261Leu
|
|
NM_001243036.1:c.782C>T
|
NP_001229965.1:p.Pro261Leu
|
|
NM_014270.4:c.782C>T
|
NP_055085.1:p.Pro261Leu
|
|
XM_006722992.1:c.101C>T
|
XP_006723055.1:p.Pro34Leu
|
|
XM_011526402.1:c.782C>T
|
XP_011524704.1:p.Pro261Leu
|
|
XM_011526402.3:c.782C>T
|
XP_011524704.1:p.Pro261Leu
|
|
XM_017026230.1:c.518C>T
|
XP_016881719.1:p.Pro173Leu
|
|
XM_024451334.1:c.155C>T
|
XP_024307102.1:p.Pro52Leu
|
|
NM_014270.5:c.782C>T
MANE Select
|
NP_055085.1:p.Pro261Leu
|
|
NM_001126335.2:c.782C>T
|
NP_001119807.1:p.Pro261Leu
|
|
NM_001243036.2:c.782C>T
|
NP_001229965.1:p.Pro261Leu
|
|