ENST00000261937.11:c.4072T>C
MANE Select
|
ENSP00000261937.6:p.Phe1358Leu
|
|
ENST00000261937.10:c.4072T>C
|
ENSP00000261937.6:p.Phe1358Leu
|
|
ENST00000502603.5:n.772T>C
|
|
|
NM_182925.4:c.4072T>C
|
NP_891555.2:p.Phe1358Leu
|
|
XM_011534477.1:c.4321T>C
|
XP_011532779.1:p.Phe1441Leu
|
|
XM_011534478.1:c.4303T>C
|
XP_011532780.1:p.Phe1435Leu
|
|
XM_011534482.1:c.4090T>C
|
XP_011532784.1:p.Phe1364Leu
|
|
XM_011534483.1:c.4012T>C
|
XP_011532785.1:p.Phe1338Leu
|
|
XM_011534484.1:c.3613T>C
|
XP_011532786.1:p.Phe1205Leu
|
|
XR_941095.1:n.4358T>C
|
|
|
XM_011534478.3:c.4303T>C
|
XP_011532780.1:p.Phe1435Leu
|
|
XM_011534484.2:c.3613T>C
|
XP_011532786.1:p.Phe1205Leu
|
|
XM_017009263.1:c.*218T>C
|
XP_016864752.1:n.*218T>C
|
|
XM_017009268.1:c.3994T>C
|
XP_016864757.1:p.Phe1332Leu
|
|
XR_001742050.2:n.4562T>C
|
|
|
NM_182925.5:c.4072T>C
MANE Select
|
NP_891555.2:p.Phe1358Leu
|
|