ENST00000703783.1:n.275G=
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|
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ENST00000703785.1:n.356G=
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|
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ENST00000262464.9:c.3491G=
MANE Select
|
ENSP00000262464.4:p.Arg1164=
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|
ENST00000262464.8:c.3491G=
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ENSP00000262464.4:p.Arg1164=
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|
ENST00000507835.5:c.41G=
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ENSP00000426839.1:p.Arg14=
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|
ENST00000508053.5:c.3491G=
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ENSP00000424571.1:p.Arg1164=
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|
ENST00000508989.5:c.3392G=
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ENSP00000425596.1:p.Arg1131=
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|
ENST00000619499.4:c.3488G=
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ENSP00000482132.1:p.Arg1163=
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|
NM_001999.3:c.3491G=
|
NP_001990.2:p.Arg1164=
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|
XM_017009228.2:c.3338G=
|
XP_016864717.1:p.Arg1113=
|
|
NM_001999.4:c.3491G=
MANE Select
|
NP_001990.2:p.Arg1164=
|
|