ENST00000255078.8:c.1864T>G
MANE Select
|
ENSP00000255078.4:p.Phe622Val
|
|
ENST00000674675.1:c.108T>G
|
|
|
ENST00000674878.1:c.108T>G
|
|
|
ENST00000674955.1:c.*581T>G
|
ENSP00000502463.1:n.*581T>G
|
|
ENST00000675118.1:c.1352T>G
|
|
|
ENST00000675389.1:n.139T>G
|
|
|
ENST00000675615.1:c.1864T>G
|
ENSP00000502413.1:p.Phe622Val
|
|
ENST00000675648.1:n.1239T>G
|
|
|
ENST00000675916.1:c.108T>G
|
|
|
ENST00000676173.1:n.2609T>G
|
|
|
ENST00000676182.1:c.295T>G
|
|
|
ENST00000676228.1:c.*1187T>G
|
ENSP00000502375.1:n.*1187T>G
|
|
ENST00000255078.7:c.1864T>G
|
ENSP00000255078.3:p.Phe622Val
|
|
ENST00000539064.5:n.1623T>G
|
|
|
ENST00000543739.5:n.857T>G
|
|
|
ENST00000545475.1:n.460T>G
|
|
|
NM_002180.2:c.1864T>G , LRG_250t1:c.1864T>G
|
NP_002171.2:p.Phe622Val
|
|
XM_005273974.2:c.853T>G
|
XP_005274031.1:p.Phe285Val
|
|
XM_005273975.2:c.736T>G
|
XP_005274032.1:p.Phe246Val
|
|
XM_011544994.1:c.631T>G
|
XP_011543296.1:p.Phe211Val
|
|
XR_949903.1:n.1966T>G
|
|
|
XM_005273975.3:c.736T>G
|
XP_005274032.1:p.Phe246Val
|
|
XM_017017669.2:c.853T>G
|
XP_016873158.1:p.Phe285Val
|
|
XM_017017670.2:c.853T>G
|
XP_016873159.1:p.Phe285Val
|
|
XR_949903.3:n.1962T>G
|
|
|
NM_002180.3:c.1864T>G
MANE Select
|
NP_002171.2:p.Phe622Val
|
|