ENST00000255078.8:c.2236T>A
MANE Select
|
ENSP00000255078.4:p.Phe746Ile
|
|
ENST00000674675.1:c.480T>A
|
|
|
ENST00000674878.1:c.480T>A
|
|
|
ENST00000674955.1:c.*953T>A
|
ENSP00000502463.1:n.*953T>A
|
|
ENST00000675118.1:c.1724T>A
|
|
|
ENST00000675389.1:n.511T>A
|
|
|
ENST00000675615.1:c.2236T>A
|
ENSP00000502413.1:p.Phe746Ile
|
|
ENST00000675648.1:n.1611T>A
|
|
|
ENST00000675916.1:c.480T>A
|
|
|
ENST00000676173.1:n.2981T>A
|
|
|
ENST00000676182.1:c.667T>A
|
|
|
ENST00000676228.1:c.*1559T>A
|
ENSP00000502375.1:n.*1559T>A
|
|
ENST00000255078.7:c.2236T>A
|
ENSP00000255078.3:p.Phe746Ile
|
|
ENST00000539064.5:n.1995T>A
|
|
|
ENST00000543739.5:n.1229T>A
|
|
|
NM_002180.2:c.2236T>A , LRG_250t1:c.2236T>A
|
NP_002171.2:p.Phe746Ile
|
|
XM_005273974.2:c.1225T>A
|
XP_005274031.1:p.Phe409Ile
|
|
XM_005273975.2:c.1108T>A
|
XP_005274032.1:p.Phe370Ile
|
|
XM_011544994.1:c.1003T>A
|
XP_011543296.1:p.Phe335Ile
|
|
XR_949903.1:n.2338T>A
|
|
|
XM_005273975.3:c.1108T>A
|
XP_005274032.1:p.Phe370Ile
|
|
XM_017017669.2:c.1225T>A
|
XP_016873158.1:p.Phe409Ile
|
|
XM_017017670.2:c.1225T>A
|
XP_016873159.1:p.Phe409Ile
|
|
XR_949903.3:n.2334T>A
|
|
|
NM_002180.3:c.2236T>A
MANE Select
|
NP_002171.2:p.Phe746Ile
|
|