ENST00000399503.4:c.2603C>T
MANE Select
|
ENSP00000382423.3:p.Ala868Val
|
|
ENST00000399503.3:c.2603C>T
|
ENSP00000382423.3:p.Ala868Val
|
|
NM_005921.1:c.2603C>T
|
NP_005912.1:p.Ala868Val
|
|
XM_005248519.3:c.2225C>T
|
XP_005248576.2:p.Ala742Val
|
|
XM_011543406.1:c.2348C>T
|
XP_011541708.1:p.Ala783Val
|
|
XM_011543407.1:c.2324C>T
|
XP_011541709.1:p.Ala775Val
|
|
XM_011543408.1:c.2603C>T
|
XP_011541710.1:p.Ala868Val
|
|
XM_017009484.1:c.2192C>T
|
XP_016864973.1:p.Ala731Val
|
|
XM_017009485.1:c.2114C>T
|
XP_016864974.1:p.Ala705Val
|
|
XR_001742068.2:n.2634C>T
|
|
|
NM_005921.2:c.2603C>T
MANE Select
|
NP_005912.1:p.Ala868Val
|
|