ENST00000261937.11:c.3939T>C
MANE Select
|
ENSP00000261937.6:p.Pro1313=
|
|
ENST00000261937.10:c.3939T>C
|
ENSP00000261937.6:p.Pro1313=
|
|
ENST00000502603.5:n.639T>C
|
|
|
NM_182925.4:c.3939T>C
|
NP_891555.2:p.Pro1313=
|
|
XM_011534477.1:c.4188T>C
|
XP_011532779.1:p.Pro1396=
|
|
XM_011534478.1:c.4170T>C
|
XP_011532780.1:p.Pro1390=
|
|
XM_011534479.1:c.*85T>C
|
XP_011532781.1:n.*85T>C
|
|
XM_011534482.1:c.3957T>C
|
XP_011532784.1:p.Pro1319=
|
|
XM_011534483.1:c.3879T>C
|
XP_011532785.1:p.Pro1293=
|
|
XM_011534484.1:c.3480T>C
|
XP_011532786.1:p.Pro1160=
|
|
XR_941095.1:n.4225T>C
|
|
|
XM_011534478.3:c.4170T>C
|
XP_011532780.1:p.Pro1390=
|
|
XM_011534484.2:c.3480T>C
|
XP_011532786.1:p.Pro1160=
|
|
XM_017009263.1:c.*85T>C
|
XP_016864752.1:n.*85T>C
|
|
XM_017009268.1:c.3861T>C
|
XP_016864757.1:p.Pro1287=
|
|
XR_001742050.2:n.4429T>C
|
|
|
NM_182925.5:c.3939T>C
MANE Select
|
NP_891555.2:p.Pro1313=
|
|