ENST00000683572.1:n.745G>T
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ENST00000341947.7:c.4939G>T
MANE Select
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ENSP00000339915.2:p.Ala1647Ser
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ENST00000341947.6:c.4939G>T
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ENSP00000339915.2:p.Ala1647Ser
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ENST00000361917.5:c.4618G>T
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ENSP00000355123.1:p.Ala1540Ser
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ENST00000374708.8:c.4681G>T
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ENSP00000363840.4:p.Ala1561Ser
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ENST00000477772.1:n.729G>T
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NM_080679.2:c.4618G>T
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NP_542410.2:p.Ala1540Ser
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NM_080680.2:c.4939G>T
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NP_542411.2:p.Ala1647Ser
|
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NM_080681.2:c.4681G>T
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NP_542412.2:p.Ala1561Ser
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XM_011514298.1:c.4093G>T
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XP_011512600.1:p.Ala1365Ser
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XM_011514299.1:c.4225G>T
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XP_011512601.1:p.Ala1409Ser
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XM_011514300.1:c.4045G>T
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XP_011512602.1:p.Ala1349Ser
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XM_011514301.1:c.3982G>T
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XP_011512603.1:p.Ala1328Ser
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XM_011514302.1:c.3826G>T
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XP_011512604.1:p.Ala1276Ser
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XM_011514299.2:c.4225G>T
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XP_011512601.1:p.Ala1409Ser
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XM_011514300.2:c.4045G>T
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XP_011512602.1:p.Ala1349Ser
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XM_011514302.2:c.3826G>T
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XP_011512604.1:p.Ala1276Ser
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XM_017010250.1:c.4939G>T
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XP_016865739.1:p.Ala1647Ser
|
|
XM_017010251.2:c.3757G>T
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XP_016865740.1:p.Ala1253Ser
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NM_080680.3:c.4939G>T
MANE Select
|
NP_542411.2:p.Ala1647Ser
|
|
NM_080681.3:c.4681G>T
|
NP_542412.2:p.Ala1561Ser
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|
NM_080679.3:c.4618G>T
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NP_542410.2:p.Ala1540Ser
|
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