ENST00000255078.8:c.2237T>C
MANE Select
|
ENSP00000255078.4:p.Phe746Ser
|
|
ENST00000674675.1:c.481T>C
|
|
|
ENST00000674878.1:c.481T>C
|
|
|
ENST00000674955.1:c.*954T>C
|
ENSP00000502463.1:n.*954T>C
|
|
ENST00000675118.1:c.1725T>C
|
|
|
ENST00000675389.1:n.512T>C
|
|
|
ENST00000675615.1:c.2237T>C
|
ENSP00000502413.1:p.Phe746Ser
|
|
ENST00000675648.1:n.1612T>C
|
|
|
ENST00000675916.1:c.481T>C
|
|
|
ENST00000676173.1:n.2982T>C
|
|
|
ENST00000676182.1:c.668T>C
|
|
|
ENST00000676228.1:c.*1560T>C
|
ENSP00000502375.1:n.*1560T>C
|
|
ENST00000255078.7:c.2237T>C
|
ENSP00000255078.3:p.Phe746Ser
|
|
ENST00000539064.5:n.1996T>C
|
|
|
ENST00000543739.5:n.1230T>C
|
|
|
NM_002180.2:c.2237T>C , LRG_250t1:c.2237T>C
|
NP_002171.2:p.Phe746Ser
|
|
XM_005273974.2:c.1226T>C
|
XP_005274031.1:p.Phe409Ser
|
|
XM_005273975.2:c.1109T>C
|
XP_005274032.1:p.Phe370Ser
|
|
XM_011544994.1:c.1004T>C
|
XP_011543296.1:p.Phe335Ser
|
|
XR_949903.1:n.2339T>C
|
|
|
XM_005273975.3:c.1109T>C
|
XP_005274032.1:p.Phe370Ser
|
|
XM_017017669.2:c.1226T>C
|
XP_016873158.1:p.Phe409Ser
|
|
XM_017017670.2:c.1226T>C
|
XP_016873159.1:p.Phe409Ser
|
|
XR_949903.3:n.2335T>C
|
|
|
NM_002180.3:c.2237T>C
MANE Select
|
NP_002171.2:p.Phe746Ser
|
|