|
ENST00000367400.8:c.2305C>A
MANE Select
|
ENSP00000356370.3:p.Arg769Ser
|
|
|
ENST00000638467.1:c.2305C>A
|
ENSP00000491102.1:p.Arg769Ser
|
|
|
ENST00000681519.1:c.1186C>A
|
ENSP00000505267.1:p.Arg396Ser
|
|
|
ENST00000367397.1:c.448C>A
|
ENSP00000356367.1:p.Arg150Ser
|
|
|
ENST00000367399.6:c.1969C>A
|
ENSP00000356369.2:p.Arg657Ser
|
|
|
ENST00000367400.7:c.2305C>A
|
ENSP00000356370.3:p.Arg769Ser
|
|
|
ENST00000480086.2:n.206C>A
|
|
|
|
ENST00000484075.5:c.2305C>A
|
ENSP00000433932.1:p.Arg769Ser
|
|
|
ENST00000535699.5:c.2098C>A
|
ENSP00000438786.1:p.Arg700Ser
|
|
|
ENST00000538660.5:c.2128+5674C>A
|
ENSP00000438091.1:n.2128+5674C>A
|
|
|
NM_001193640.1:c.1969C>A
|
NP_001180569.1:p.Arg657Ser
|
|
|
NM_001257965.1:c.2098C>A
|
NP_001244894.1:p.Arg700Ser
|
|
|
NM_001257966.1:c.2128+5674C>A
|
NP_001244895.1:n.2128+5674C>A
|
|
|
NM_201253.2:c.2305C>A
|
NP_957705.1:p.Arg769Ser
|
|
|
NR_047563.1:n.2306C>A
|
|
|
|
NR_047564.1:n.2514C>A
|
|
|
|
XM_011509365.1:c.2305C>A
|
XP_011507667.1:p.Arg769Ser
|
|
|
XM_011509366.1:c.2305C>A
|
XP_011507668.1:p.Arg769Ser
|
|
|
XM_011509367.1:c.2305C>A
|
XP_011507669.1:p.Arg769Ser
|
|
|
XM_011509368.1:c.1723C>A
|
XP_011507670.1:p.Arg575Ser
|
|
|
XM_011509369.1:c.748C>A
|
XP_011507671.1:p.Arg250Ser
|
|
|
XM_011509365.2:c.2305C>A
|
XP_011507667.1:p.Arg769Ser
|
|
|
XM_011509369.2:c.748C>A
|
XP_011507671.1:p.Arg250Ser
|
|
|
XM_017000851.1:c.1462C>A
|
XP_016856340.1:p.Arg488Ser
|
|
|
XM_017000852.1:c.2305C>A
|
XP_016856341.1:p.Arg769Ser
|
|
|
NM_201253.3:c.2305C>A
MANE Select
|
NP_957705.1:p.Arg769Ser
|
|
|
NM_001193640.2:c.1969C>A
|
NP_001180569.1:p.Arg657Ser
|
|
|
NM_001257965.2:c.2098C>A
|
NP_001244894.1:p.Arg700Ser
|
|
|
NR_047563.2:n.2258C>A
|
|
|
|
NR_047564.2:n.2466C>A
|
|
|
|
NM_001257966.2:c.2128+5674C>A
|
NP_001244895.1:n.2128+5674C>A
|
|
