ENST00000485303.6:c.843T>C
MANE Select
|
ENSP00000418070.1:p.Phe281=
|
|
ENST00000319792.7:c.843T>C
|
ENSP00000321514.3:p.Phe281=
|
|
ENST00000485303.5:c.843T>C
|
ENSP00000418070.1:p.Phe281=
|
|
ENST00000486596.5:c.544T>C
|
|
|
ENST00000493615.5:c.774T>C
|
ENSP00000420579.1:p.Phe258=
|
|
NM_001243286.1:c.843T>C
|
NP_001230215.1:p.Phe281=
|
|
NM_001243288.1:c.774T>C
|
NP_001230217.1:p.Phe258=
|
|
NM_015480.2:c.843T>C
|
NP_056295.1:p.Phe281=
|
|
XM_005247322.3:c.843T>C
|
XP_005247379.2:p.Phe281=
|
|
XM_011512662.1:c.936T>C
|
XP_011510964.1:p.Phe312=
|
|
XM_011512663.1:c.936T>C
|
XP_011510965.1:p.Phe312=
|
|
XM_011512664.1:c.774T>C
|
XP_011510966.1:p.Phe258=
|
|
XM_011512665.1:c.936T>C
|
XP_011510967.1:p.Phe312=
|
|
XM_011512666.1:c.936T>C
|
XP_011510968.1:p.Phe312=
|
|
XM_011512667.1:c.207T>C
|
XP_011510969.1:p.Phe69=
|
|
XR_924122.1:n.1166T>C
|
|
|
XM_017006123.1:c.936T>C
|
XP_016861612.1:p.Phe312=
|
|
XM_017006124.1:c.798T>C
|
XP_016861613.1:p.Phe266=
|
|
XM_017006125.1:c.774T>C
|
XP_016861614.1:p.Phe258=
|
|
XM_017006126.1:c.843T>C
|
XP_016861615.1:p.Phe281=
|
|
XM_017006127.2:c.207T>C
|
XP_016861616.1:p.Phe69=
|
|
XR_002959508.1:n.1124T>C
|
|
|
XR_924122.2:n.1166T>C
|
|
|
NM_015480.3:c.843T>C
MANE Select
|
NP_056295.1:p.Phe281=
|
|
NM_001243286.2:c.843T>C
|
NP_001230215.1:p.Phe281=
|
|
NM_001243288.2:c.774T>C
|
NP_001230217.1:p.Phe258=
|
|