ENST00000255078.8:c.2359C>G
MANE Select
|
ENSP00000255078.4:p.Pro787Ala
|
|
ENST00000674675.1:c.587+16C>G
|
|
|
ENST00000674878.1:c.547+56C>G
|
|
|
ENST00000674955.1:c.*1076C>G
|
ENSP00000502463.1:n.*1076C>G
|
|
ENST00000675118.1:c.1847C>G
|
|
|
ENST00000675389.1:n.634C>G
|
|
|
ENST00000675615.1:c.2359C>G
|
ENSP00000502413.1:p.Pro787Ala
|
|
ENST00000675648.1:n.1734C>G
|
|
|
ENST00000675916.1:c.603C>G
|
|
|
ENST00000676173.1:n.3104C>G
|
|
|
ENST00000676182.1:c.790C>G
|
|
|
ENST00000676228.1:c.*1682C>G
|
ENSP00000502375.1:n.*1682C>G
|
|
ENST00000255078.7:c.2359C>G
|
ENSP00000255078.3:p.Pro787Ala
|
|
ENST00000539064.5:n.2118C>G
|
|
|
ENST00000543739.5:n.1352C>G
|
|
|
NM_002180.2:c.2359C>G , LRG_250t1:c.2359C>G
|
NP_002171.2:p.Pro787Ala
|
|
XM_005273974.2:c.1348C>G
|
XP_005274031.1:p.Pro450Ala
|
|
XM_005273975.2:c.1231C>G
|
XP_005274032.1:p.Pro411Ala
|
|
XM_011544994.1:c.1126C>G
|
XP_011543296.1:p.Pro376Ala
|
|
XR_949903.1:n.2461C>G
|
|
|
XM_005273975.3:c.1231C>G
|
XP_005274032.1:p.Pro411Ala
|
|
XM_017017669.2:c.1348C>G
|
XP_016873158.1:p.Pro450Ala
|
|
XM_017017670.2:c.1348C>G
|
XP_016873159.1:p.Pro450Ala
|
|
XR_949903.3:n.2457C>G
|
|
|
NM_002180.3:c.2359C>G
MANE Select
|
NP_002171.2:p.Pro787Ala
|
|