ENST00000366777.4:c.1241G>A
MANE Select
|
ENSP00000355739.3:p.Cys414Tyr
|
|
ENST00000366779.6:c.*5968G>A
|
ENSP00000355741.2:n.*5968G>A
|
|
ENST00000676884.1:c.*6090G>A
|
ENSP00000503200.1:n.*6090G>A
|
|
ENST00000366777.3:c.1241G>A
|
ENSP00000355739.3:p.Cys414Tyr
|
|
ENST00000366778.5:c.1085G>A
|
ENSP00000355740.1:p.Cys362Tyr
|
|
ENST00000366779.5:c.1241G>A
|
ENSP00000355741.1:p.Cys414Tyr
|
|
ENST00000478406.5:n.1864G>A
|
|
|
ENST00000479852.1:n.189G>A
|
|
|
ENST00000485462.5:n.631G>A
|
|
|
NM_020247.4:c.1241G>A
|
NP_064632.2:p.Cys414Tyr
|
|
XM_005273201.1:c.1241G>A
|
XP_005273258.1:p.Cys414Tyr
|
|
XM_011544238.1:c.1241G>A
|
XP_011542540.1:p.Cys414Tyr
|
|
XM_011544239.1:c.1241G>A
|
XP_011542541.1:p.Cys414Tyr
|
|
XM_011544240.1:c.1241G>A
|
XP_011542542.1:p.Cys414Tyr
|
|
XM_011544241.1:c.1241G>A
|
XP_011542543.1:p.Cys414Tyr
|
|
XM_011544239.2:c.1241G>A
|
XP_011542541.1:p.Cys414Tyr
|
|
XM_011544241.2:c.1241G>A
|
XP_011542543.1:p.Cys414Tyr
|
|
XM_017001852.1:c.1241G>A
|
XP_016857341.1:p.Cys414Tyr
|
|
XM_024448517.1:c.1241G>A
|
XP_024304285.1:p.Cys414Tyr
|
|
XM_024448518.1:c.1241G>A
|
XP_024304286.1:p.Cys414Tyr
|
|
NM_020247.5:c.1241G>A
MANE Select
|
NP_064632.2:p.Cys414Tyr
|
|