|
ENST00000216465.10:c.163C>A
MANE Select
|
ENSP00000216465.5:p.Pro55Thr
|
|
|
ENST00000216465.9:c.163C>A
|
ENSP00000216465.5:p.Pro55Thr
|
|
|
ENST00000349555.7:c.163C>A
|
ENSP00000314404.5:p.Pro55Thr
|
|
|
ENST00000361389.8:c.-3C>A
|
ENSP00000354959.4:n.-3C>A
|
|
|
ENST00000393734.5:c.-3C>A
|
ENSP00000377335.1:n.-3C>A
|
|
|
ENST00000553431.5:n.294C>A
|
|
|
|
ENST00000553586.5:c.166C>A
|
ENSP00000451976.1:p.Pro56Thr
|
|
|
ENST00000553838.5:n.333C>A
|
|
|
|
ENST00000554279.5:c.163C>A
|
ENSP00000452498.1:p.Pro55Thr
|
|
|
ENST00000554846.5:c.-3C>A
|
ENSP00000452531.1:n.-3C>A
|
|
|
ENST00000555093.1:n.4212C>A
|
|
|
|
ENST00000555583.1:c.-3C>A
|
ENSP00000452346.1:n.-3C>A
|
|
|
ENST00000556627.5:c.136-413C>A
|
ENSP00000450487.1:n.136-413C>A
|
|
|
ENST00000556914.5:n.243C>A
|
|
|
|
ENST00000557053.5:c.-3C>A
|
ENSP00000451150.1:n.-3C>A
|
|
|
ENST00000557639.5:c.-3C>A
|
ENSP00000451927.1:n.-3C>A
|
|
|
NM_001312660.1:c.-3C>A
|
NP_001299589.1:n.-3C>A
|
|
|
NM_001513.3:c.-3C>A
|
NP_001504.2:n.-3C>A
|
|
|
NM_145870.2:c.163C>A
|
NP_665877.1:p.Pro55Thr
|
|
|
NM_145871.2:c.163C>A
|
NP_665878.2:p.Pro55Thr
|
|
|
XM_005267559.2:c.-3C>A
|
XP_005267616.1:n.-3C>A
|
|
|
XM_011536670.1:c.-314C>A
|
XP_011534972.1:n.-314C>A
|
|
|
XM_011536671.1:c.166C>A
|
XP_011534973.1:p.Pro56Thr
|
|
|
NM_001363703.1:c.166C>A
|
NP_001350632.1:p.Pro56Thr
|
|
|
XM_011536670.2:c.-314C>A
|
XP_011534972.1:n.-314C>A
|
|
|
XM_011536671.2:c.166C>A
|
XP_011534973.1:p.Pro56Thr
|
|
|
XM_024449549.1:c.-314C>A
|
XP_024305317.1:n.-314C>A
|
|
|
XM_024449550.1:c.-3C>A
|
XP_024305318.1:n.-3C>A
|
|
|
XM_024449551.1:c.-3C>A
|
XP_024305319.1:n.-3C>A
|
|
|
XM_024449552.1:c.-3C>A
|
XP_024305320.1:n.-3C>A
|
|
|
NM_145870.3:c.163C>A
MANE Select
|
NP_665877.1:p.Pro55Thr
|
|
|
NM_001312660.2:c.-3C>A
|
NP_001299589.1:n.-3C>A
|
|
|
NM_001363703.2:c.166C>A
|
NP_001350632.1:p.Pro56Thr
|
|
|
NM_145871.3:c.163C>A
|
NP_665878.2:p.Pro55Thr
|
|
