ENST00000683572.1:n.596A>G
|
|
|
ENST00000341947.7:c.4790A>G
MANE Select
|
ENSP00000339915.2:p.Asp1597Gly
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ENST00000341947.6:c.4790A>G
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ENSP00000339915.2:p.Asp1597Gly
|
|
ENST00000361917.5:c.4469A>G
|
ENSP00000355123.1:p.Asp1490Gly
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ENST00000374708.8:c.4532A>G
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ENSP00000363840.4:p.Asp1511Gly
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ENST00000477772.1:n.580A>G
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|
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NM_080679.2:c.4469A>G
|
NP_542410.2:p.Asp1490Gly
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NM_080680.2:c.4790A>G
|
NP_542411.2:p.Asp1597Gly
|
|
NM_080681.2:c.4532A>G
|
NP_542412.2:p.Asp1511Gly
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|
XM_011514298.1:c.3944A>G
|
XP_011512600.1:p.Asp1315Gly
|
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XM_011514299.1:c.4076A>G
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XP_011512601.1:p.Asp1359Gly
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XM_011514300.1:c.3896A>G
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XP_011512602.1:p.Asp1299Gly
|
|
XM_011514301.1:c.3833A>G
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XP_011512603.1:p.Asp1278Gly
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XM_011514302.1:c.3677A>G
|
XP_011512604.1:p.Asp1226Gly
|
|
XM_011514299.2:c.4076A>G
|
XP_011512601.1:p.Asp1359Gly
|
|
XM_011514300.2:c.3896A>G
|
XP_011512602.1:p.Asp1299Gly
|
|
XM_011514302.2:c.3677A>G
|
XP_011512604.1:p.Asp1226Gly
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|
XM_017010250.1:c.4790A>G
|
XP_016865739.1:p.Asp1597Gly
|
|
XM_017010251.2:c.3608A>G
|
XP_016865740.1:p.Asp1203Gly
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|
NM_080680.3:c.4790A>G
MANE Select
|
NP_542411.2:p.Asp1597Gly
|
|
NM_080681.3:c.4532A>G
|
NP_542412.2:p.Asp1511Gly
|
|
NM_080679.3:c.4469A>G
|
NP_542410.2:p.Asp1490Gly
|
|