ENST00000255078.8:c.1435G>C
MANE Select
|
ENSP00000255078.4:p.Ala479Pro
|
|
ENST00000674955.1:c.*152G>C
|
ENSP00000502463.1:n.*152G>C
|
|
ENST00000675118.1:c.923G>C
|
|
|
ENST00000675205.1:n.183+330G>C
|
|
|
ENST00000675615.1:c.1435G>C
|
ENSP00000502413.1:p.Ala479Pro
|
|
ENST00000675648.1:n.810G>C
|
|
|
ENST00000675997.1:n.113-653G>C
|
|
|
ENST00000676173.1:n.2180G>C
|
|
|
ENST00000676228.1:c.*758G>C
|
ENSP00000502375.1:n.*758G>C
|
|
ENST00000255078.7:c.1435G>C
|
ENSP00000255078.3:p.Ala479Pro
|
|
ENST00000537458.5:n.552G>C
|
|
|
ENST00000539064.5:n.1194G>C
|
|
|
ENST00000541229.5:n.130G>C
|
|
|
ENST00000543739.5:n.552G>C
|
|
|
NM_002180.2:c.1435G>C , LRG_250t1:c.1435G>C
|
NP_002171.2:p.Ala479Pro
|
|
XM_005273974.2:c.424G>C
|
XP_005274031.1:p.Ala142Pro
|
|
XM_005273975.2:c.307G>C
|
XP_005274032.1:p.Ala103Pro
|
|
XM_011544994.1:c.202G>C
|
XP_011543296.1:p.Ala68Pro
|
|
XR_949903.1:n.1537G>C
|
|
|
XM_005273975.3:c.307G>C
|
XP_005274032.1:p.Ala103Pro
|
|
XM_017017669.2:c.424G>C
|
XP_016873158.1:p.Ala142Pro
|
|
XM_017017670.2:c.424G>C
|
XP_016873159.1:p.Ala142Pro
|
|
XM_017017671.2:c.1435G>C
|
XP_016873160.1:p.Ala479Pro
|
|
XR_949903.3:n.1533G>C
|
|
|
NM_002180.3:c.1435G>C
MANE Select
|
NP_002171.2:p.Ala479Pro
|
|