ENST00000261937.11:c.3944C>T
MANE Select
|
ENSP00000261937.6:p.Ser1315Phe
|
|
ENST00000261937.10:c.3944C>T
|
ENSP00000261937.6:p.Ser1315Phe
|
|
ENST00000502603.5:n.644C>T
|
|
|
NM_182925.4:c.3944C>T
|
NP_891555.2:p.Ser1315Phe
|
|
XM_011534477.1:c.4193C>T
|
XP_011532779.1:p.Ser1398Phe
|
|
XM_011534478.1:c.4175C>T
|
XP_011532780.1:p.Ser1392Phe
|
|
XM_011534479.1:c.*90C>T
|
XP_011532781.1:n.*90C>T
|
|
XM_011534482.1:c.3962C>T
|
XP_011532784.1:p.Ser1321Phe
|
|
XM_011534483.1:c.3884C>T
|
XP_011532785.1:p.Ser1295Phe
|
|
XM_011534484.1:c.3485C>T
|
XP_011532786.1:p.Ser1162Phe
|
|
XR_941095.1:n.4230C>T
|
|
|
XM_011534478.3:c.4175C>T
|
XP_011532780.1:p.Ser1392Phe
|
|
XM_011534484.2:c.3485C>T
|
XP_011532786.1:p.Ser1162Phe
|
|
XM_017009263.1:c.*90C>T
|
XP_016864752.1:n.*90C>T
|
|
XM_017009268.1:c.3866C>T
|
XP_016864757.1:p.Ser1289Phe
|
|
XR_001742050.2:n.4434C>T
|
|
|
NM_182925.5:c.3944C>T
MANE Select
|
NP_891555.2:p.Ser1315Phe
|
|