ENST00000683572.1:n.657T>G
|
|
|
ENST00000341947.7:c.4851T>G
MANE Select
|
ENSP00000339915.2:p.Asp1617Glu
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ENST00000341947.6:c.4851T>G
|
ENSP00000339915.2:p.Asp1617Glu
|
|
ENST00000361917.5:c.4530T>G
|
ENSP00000355123.1:p.Asp1510Glu
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ENST00000374708.8:c.4593T>G
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ENSP00000363840.4:p.Asp1531Glu
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ENST00000477772.1:n.641T>G
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|
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NM_080679.2:c.4530T>G
|
NP_542410.2:p.Asp1510Glu
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NM_080680.2:c.4851T>G
|
NP_542411.2:p.Asp1617Glu
|
|
NM_080681.2:c.4593T>G
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NP_542412.2:p.Asp1531Glu
|
|
XM_011514298.1:c.4005T>G
|
XP_011512600.1:p.Asp1335Glu
|
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XM_011514299.1:c.4137T>G
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XP_011512601.1:p.Asp1379Glu
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XM_011514300.1:c.3957T>G
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XP_011512602.1:p.Asp1319Glu
|
|
XM_011514301.1:c.3894T>G
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XP_011512603.1:p.Asp1298Glu
|
|
XM_011514302.1:c.3738T>G
|
XP_011512604.1:p.Asp1246Glu
|
|
XM_011514299.2:c.4137T>G
|
XP_011512601.1:p.Asp1379Glu
|
|
XM_011514300.2:c.3957T>G
|
XP_011512602.1:p.Asp1319Glu
|
|
XM_011514302.2:c.3738T>G
|
XP_011512604.1:p.Asp1246Glu
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|
XM_017010250.1:c.4851T>G
|
XP_016865739.1:p.Asp1617Glu
|
|
XM_017010251.2:c.3669T>G
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XP_016865740.1:p.Asp1223Glu
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|
NM_080680.3:c.4851T>G
MANE Select
|
NP_542411.2:p.Asp1617Glu
|
|
NM_080681.3:c.4593T>G
|
NP_542412.2:p.Asp1531Glu
|
|
NM_080679.3:c.4530T>G
|
NP_542410.2:p.Asp1510Glu
|
|