ENST00000399503.4:c.2593A>G
MANE Select
|
ENSP00000382423.3:p.Ile865Val
|
|
ENST00000399503.3:c.2593A>G
|
ENSP00000382423.3:p.Ile865Val
|
|
NM_005921.1:c.2593A>G
|
NP_005912.1:p.Ile865Val
|
|
XM_005248519.3:c.2215A>G
|
XP_005248576.2:p.Ile739Val
|
|
XM_011543406.1:c.2338A>G
|
XP_011541708.1:p.Ile780Val
|
|
XM_011543407.1:c.2314A>G
|
XP_011541709.1:p.Ile772Val
|
|
XM_011543408.1:c.2593A>G
|
XP_011541710.1:p.Ile865Val
|
|
XM_017009484.1:c.2182A>G
|
XP_016864973.1:p.Ile728Val
|
|
XM_017009485.1:c.2104A>G
|
XP_016864974.1:p.Ile702Val
|
|
XR_001742068.2:n.2624A>G
|
|
|
NM_005921.2:c.2593A>G
MANE Select
|
NP_005912.1:p.Ile865Val
|
|