ENST00000683572.1:n.726G>C
|
|
|
ENST00000341947.7:c.4920G>C
MANE Select
|
ENSP00000339915.2:p.Leu1640=
|
|
ENST00000341947.6:c.4920G>C
|
ENSP00000339915.2:p.Leu1640=
|
|
ENST00000361917.5:c.4599G>C
|
ENSP00000355123.1:p.Leu1533=
|
|
ENST00000374708.8:c.4662G>C
|
ENSP00000363840.4:p.Leu1554=
|
|
ENST00000477772.1:n.710G>C
|
|
|
NM_080679.2:c.4599G>C
|
NP_542410.2:p.Leu1533=
|
|
NM_080680.2:c.4920G>C
|
NP_542411.2:p.Leu1640=
|
|
NM_080681.2:c.4662G>C
|
NP_542412.2:p.Leu1554=
|
|
XM_011514298.1:c.4074G>C
|
XP_011512600.1:p.Leu1358=
|
|
XM_011514299.1:c.4206G>C
|
XP_011512601.1:p.Leu1402=
|
|
XM_011514300.1:c.4026G>C
|
XP_011512602.1:p.Leu1342=
|
|
XM_011514301.1:c.3963G>C
|
XP_011512603.1:p.Leu1321=
|
|
XM_011514302.1:c.3807G>C
|
XP_011512604.1:p.Leu1269=
|
|
XM_011514299.2:c.4206G>C
|
XP_011512601.1:p.Leu1402=
|
|
XM_011514300.2:c.4026G>C
|
XP_011512602.1:p.Leu1342=
|
|
XM_011514302.2:c.3807G>C
|
XP_011512604.1:p.Leu1269=
|
|
XM_017010250.1:c.4920G>C
|
XP_016865739.1:p.Leu1640=
|
|
XM_017010251.2:c.3738G>C
|
XP_016865740.1:p.Leu1246=
|
|
NM_080680.3:c.4920G>C
MANE Select
|
NP_542411.2:p.Leu1640=
|
|
NM_080681.3:c.4662G>C
|
NP_542412.2:p.Leu1554=
|
|
NM_080679.3:c.4599G>C
|
NP_542410.2:p.Leu1533=
|
|