ENST00000399503.4:c.1759C>T
MANE Select
|
ENSP00000382423.3:p.Leu587Phe
|
|
ENST00000399503.3:c.1759C>T
|
ENSP00000382423.3:p.Leu587Phe
|
|
NM_005921.1:c.1759C>T
|
NP_005912.1:p.Leu587Phe
|
|
XM_005248519.3:c.1381C>T
|
XP_005248576.2:p.Leu461Phe
|
|
XM_011543406.1:c.1504C>T
|
XP_011541708.1:p.Leu502Phe
|
|
XM_011543407.1:c.1686+2099C>T
|
XP_011541709.1:n.1686+2099C>T
|
|
XM_011543408.1:c.1759C>T
|
XP_011541710.1:p.Leu587Phe
|
|
XM_017009484.1:c.1348C>T
|
XP_016864973.1:p.Leu450Phe
|
|
XM_017009485.1:c.1270C>T
|
XP_016864974.1:p.Leu424Phe
|
|
XR_001742068.2:n.1790C>T
|
|
|
NM_005921.2:c.1759C>T
MANE Select
|
NP_005912.1:p.Leu587Phe
|
|