ENST00000683572.1:n.680T>A
|
|
|
ENST00000341947.7:c.4874T>A
MANE Select
|
ENSP00000339915.2:p.Val1625Glu
|
|
ENST00000341947.6:c.4874T>A
|
ENSP00000339915.2:p.Val1625Glu
|
|
ENST00000361917.5:c.4553T>A
|
ENSP00000355123.1:p.Val1518Glu
|
|
ENST00000374708.8:c.4616T>A
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ENSP00000363840.4:p.Val1539Glu
|
|
ENST00000477772.1:n.664T>A
|
|
|
NM_080679.2:c.4553T>A
|
NP_542410.2:p.Val1518Glu
|
|
NM_080680.2:c.4874T>A
|
NP_542411.2:p.Val1625Glu
|
|
NM_080681.2:c.4616T>A
|
NP_542412.2:p.Val1539Glu
|
|
XM_011514298.1:c.4028T>A
|
XP_011512600.1:p.Val1343Glu
|
|
XM_011514299.1:c.4160T>A
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XP_011512601.1:p.Val1387Glu
|
|
XM_011514300.1:c.3980T>A
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XP_011512602.1:p.Val1327Glu
|
|
XM_011514301.1:c.3917T>A
|
XP_011512603.1:p.Val1306Glu
|
|
XM_011514302.1:c.3761T>A
|
XP_011512604.1:p.Val1254Glu
|
|
XM_011514299.2:c.4160T>A
|
XP_011512601.1:p.Val1387Glu
|
|
XM_011514300.2:c.3980T>A
|
XP_011512602.1:p.Val1327Glu
|
|
XM_011514302.2:c.3761T>A
|
XP_011512604.1:p.Val1254Glu
|
|
XM_017010250.1:c.4874T>A
|
XP_016865739.1:p.Val1625Glu
|
|
XM_017010251.2:c.3692T>A
|
XP_016865740.1:p.Val1231Glu
|
|
NM_080680.3:c.4874T>A
MANE Select
|
NP_542411.2:p.Val1625Glu
|
|
NM_080681.3:c.4616T>A
|
NP_542412.2:p.Val1539Glu
|
|
NM_080679.3:c.4553T>A
|
NP_542410.2:p.Val1518Glu
|
|