ENST00000262027.10:c.1619G>A
MANE Select
|
ENSP00000262027.5:p.Trp540Ter
|
|
ENST00000262027.9:c.1619G>A
|
ENSP00000262027.5:p.Trp540Ter
|
|
ENST00000447721.6:n.1261G>A
|
|
|
ENST00000537638.6:c.1619G>A
|
ENSP00000446168.2:p.Trp540Ter
|
|
ENST00000545888.6:c.*1120G>A
|
ENSP00000439307.2:n.*1120G>A
|
|
ENST00000546971.5:n.363G>A
|
|
|
ENST00000548630.1:n.180G>A
|
|
|
ENST00000548944.1:c.134-4408G>A
|
ENSP00000449071.1:n.134-4408G>A
|
|
ENST00000549048.1:n.152G>A
|
|
|
ENST00000628866.2:c.*1120G>A
|
ENSP00000486738.1:n.*1120G>A
|
|
NM_004990.3:c.1619G>A
|
NP_004981.2:p.Trp540Ter
|
|
XM_006719398.2:c.917G>A
|
XP_006719461.1:p.Trp306Ter
|
|
XM_011538353.1:c.1619G>A
|
XP_011536655.1:p.Trp540Ter
|
|
XM_006719398.4:c.917G>A
|
XP_006719461.1:p.Trp306Ter
|
|
XR_001748704.2:n.1642G>A
|
|
|
XR_002957327.1:n.1566G>A
|
|
|
NM_004990.4:c.1619G>A
MANE Select
|
NP_004981.2:p.Trp540Ter
|
|