ENST00000297598.5:c.1594G=
MANE Select
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ENSP00000297598.4:p.Ala532=
|
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ENST00000297598.4:c.1594G=
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ENSP00000297598.4:p.Ala532=
|
|
ENST00000396200.3:c.1669G=
|
ENSP00000379503.3:p.Ala557=
|
|
ENST00000517764.1:c.1594G=
|
ENSP00000430380.1:p.Ala532=
|
|
ENST00000520728.5:c.1594G=
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ENSP00000428317.1:p.Ala532=
|
|
NM_001161779.1:c.1669G=
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NP_001155251.1:p.Ala557=
|
|
NM_001161780.1:c.1669G=
|
NP_001155252.1:p.Ala557=
|
|
NM_001161781.1:c.1594G=
|
NP_001155253.1:p.Ala532=
|
|
NM_018444.3:c.1594G=
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NP_060914.2:p.Ala532=
|
|
XM_011517135.1:c.1648G=
|
XP_011515437.1:p.Ala550=
|
|
XM_011517136.1:c.1594G=
|
XP_011515438.1:p.Ala532=
|
|
XM_011517137.1:c.1594G=
|
XP_011515439.1:p.Ala532=
|
|
XM_011517135.2:c.1648G=
|
XP_011515437.1:p.Ala550=
|
|
XM_011517136.2:c.1594G=
|
XP_011515438.1:p.Ala532=
|
|
XM_017013588.1:c.1756G=
|
XP_016869077.1:p.Ala586=
|
|
NM_018444.4:c.1594G=
MANE Select
|
NP_060914.2:p.Ala532=
|
|
NM_001161780.2:c.1669G=
|
NP_001155252.1:p.Ala557=
|
|
NM_001161781.2:c.1594G=
|
NP_001155253.1:p.Ala532=
|
|
NM_001161779.2:c.1669G=
|
NP_001155251.1:p.Ala557=
|
|