ENST00000255078.8:c.2130C>A
MANE Select
|
ENSP00000255078.4:p.Pro710=
|
|
ENST00000674675.1:c.374C>A
|
|
|
ENST00000674878.1:c.374C>A
|
|
|
ENST00000674955.1:c.*847C>A
|
ENSP00000502463.1:n.*847C>A
|
|
ENST00000675118.1:c.1618C>A
|
|
|
ENST00000675389.1:n.405C>A
|
|
|
ENST00000675615.1:c.2130C>A
|
ENSP00000502413.1:p.Pro710=
|
|
ENST00000675648.1:n.1505C>A
|
|
|
ENST00000675916.1:c.374C>A
|
|
|
ENST00000676173.1:n.2875C>A
|
|
|
ENST00000676182.1:c.561C>A
|
|
|
ENST00000676228.1:c.*1453C>A
|
ENSP00000502375.1:n.*1453C>A
|
|
ENST00000255078.7:c.2130C>A
|
ENSP00000255078.3:p.Pro710=
|
|
ENST00000539064.5:n.1889C>A
|
|
|
ENST00000543739.5:n.1123C>A
|
|
|
NM_002180.2:c.2130C>A , LRG_250t1:c.2130C>A
|
NP_002171.2:p.Pro710=
|
|
XM_005273974.2:c.1119C>A
|
XP_005274031.1:p.Pro373=
|
|
XM_005273975.2:c.1002C>A
|
XP_005274032.1:p.Pro334=
|
|
XM_011544994.1:c.897C>A
|
XP_011543296.1:p.Pro299=
|
|
XR_949903.1:n.2232C>A
|
|
|
XM_005273975.3:c.1002C>A
|
XP_005274032.1:p.Pro334=
|
|
XM_017017669.2:c.1119C>A
|
XP_016873158.1:p.Pro373=
|
|
XM_017017670.2:c.1119C>A
|
XP_016873159.1:p.Pro373=
|
|
XR_949903.3:n.2228C>A
|
|
|
NM_002180.3:c.2130C>A
MANE Select
|
NP_002171.2:p.Pro710=
|
|