ENST00000683572.1:n.747C>G
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|
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ENST00000341947.7:c.4941C>G
MANE Select
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ENSP00000339915.2:p.Ala1647=
|
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ENST00000341947.6:c.4941C>G
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ENSP00000339915.2:p.Ala1647=
|
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ENST00000361917.5:c.4620C>G
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ENSP00000355123.1:p.Ala1540=
|
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ENST00000374708.8:c.4683C>G
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ENSP00000363840.4:p.Ala1561=
|
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ENST00000477772.1:n.731C>G
|
|
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NM_080679.2:c.4620C>G
|
NP_542410.2:p.Ala1540=
|
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NM_080680.2:c.4941C>G
|
NP_542411.2:p.Ala1647=
|
|
NM_080681.2:c.4683C>G
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NP_542412.2:p.Ala1561=
|
|
XM_011514298.1:c.4095C>G
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XP_011512600.1:p.Ala1365=
|
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XM_011514299.1:c.4227C>G
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XP_011512601.1:p.Ala1409=
|
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XM_011514300.1:c.4047C>G
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XP_011512602.1:p.Ala1349=
|
|
XM_011514301.1:c.3984C>G
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XP_011512603.1:p.Ala1328=
|
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XM_011514302.1:c.3828C>G
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XP_011512604.1:p.Ala1276=
|
|
XM_011514299.2:c.4227C>G
|
XP_011512601.1:p.Ala1409=
|
|
XM_011514300.2:c.4047C>G
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XP_011512602.1:p.Ala1349=
|
|
XM_011514302.2:c.3828C>G
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XP_011512604.1:p.Ala1276=
|
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XM_017010250.1:c.4941C>G
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XP_016865739.1:p.Ala1647=
|
|
XM_017010251.2:c.3759C>G
|
XP_016865740.1:p.Ala1253=
|
|
NM_080680.3:c.4941C>G
MANE Select
|
NP_542411.2:p.Ala1647=
|
|
NM_080681.3:c.4683C>G
|
NP_542412.2:p.Ala1561=
|
|
NM_080679.3:c.4620C>G
|
NP_542410.2:p.Ala1540=
|
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