ENST00000261937.11:c.3926C>T
MANE Select
|
ENSP00000261937.6:p.Thr1309Ile
|
|
ENST00000261937.10:c.3926C>T
|
ENSP00000261937.6:p.Thr1309Ile
|
|
ENST00000502603.5:n.626C>T
|
|
|
NM_182925.4:c.3926C>T
|
NP_891555.2:p.Thr1309Ile
|
|
XM_011534477.1:c.4175C>T
|
XP_011532779.1:p.Thr1392Ile
|
|
XM_011534478.1:c.4157C>T
|
XP_011532780.1:p.Thr1386Ile
|
|
XM_011534479.1:c.*72C>T
|
XP_011532781.1:n.*72C>T
|
|
XM_011534482.1:c.3944C>T
|
XP_011532784.1:p.Thr1315Ile
|
|
XM_011534483.1:c.3866C>T
|
XP_011532785.1:p.Thr1289Ile
|
|
XM_011534484.1:c.3467C>T
|
XP_011532786.1:p.Thr1156Ile
|
|
XR_941095.1:n.4212C>T
|
|
|
XM_011534478.3:c.4157C>T
|
XP_011532780.1:p.Thr1386Ile
|
|
XM_011534484.2:c.3467C>T
|
XP_011532786.1:p.Thr1156Ile
|
|
XM_017009263.1:c.*72C>T
|
XP_016864752.1:n.*72C>T
|
|
XM_017009268.1:c.3848C>T
|
XP_016864757.1:p.Thr1283Ile
|
|
XR_001742050.2:n.4416C>T
|
|
|
NM_182925.5:c.3926C>T
MANE Select
|
NP_891555.2:p.Thr1309Ile
|
|