ENST00000382103.7:c.981G>C
MANE Select
|
ENSP00000371535.2:p.Leu327Phe
|
|
ENST00000680581.1:c.981G>C
|
ENSP00000506483.1:p.Leu327Phe
|
|
ENST00000680824.1:n.2197G>C
|
|
|
ENST00000681071.1:n.1273G>C
|
|
|
ENST00000681341.1:n.2122G>C
|
|
|
ENST00000681948.1:c.1236G>C
|
ENSP00000505991.1:p.Leu412Phe
|
|
ENST00000358971.7:c.*779G>C
|
ENSP00000351857.3:n.*779G>C
|
|
ENST00000382103.6:c.981G>C
|
ENSP00000371535.2:p.Leu327Phe
|
|
ENST00000503150.1:c.263G>C
|
|
|
ENST00000505513.1:n.281G>C
|
|
|
ENST00000514585.5:c.*682G>C
|
ENSP00000421880.1:n.*682G>C
|
|
NM_016955.3:c.981G>C
|
NP_058651.3:p.Leu327Phe
|
|
XM_005248168.2:c.744G>C
|
XP_005248225.1:p.Leu248Phe
|
|
XM_006713965.2:c.801G>C
|
XP_006714028.1:p.Leu267Phe
|
|
XM_011513846.1:c.978G>C
|
XP_011512148.1:p.Leu326Phe
|
|
XM_011513847.1:c.948G>C
|
XP_011512149.1:p.Leu316Phe
|
|
XM_011513848.1:c.801G>C
|
XP_011512150.1:p.Leu267Phe
|
|
XM_011513846.2:c.978G>C
|
XP_011512148.1:p.Leu326Phe
|
|
XM_011513847.2:c.948G>C
|
XP_011512149.1:p.Leu316Phe
|
|
XM_017008277.1:c.1236G>C
|
XP_016863766.1:p.Leu412Phe
|
|
XM_017008278.1:c.558G>C
|
XP_016863767.1:p.Leu186Phe
|
|
NM_016955.4:c.981G>C
MANE Select
|
NP_058651.3:p.Leu327Phe
|
|