ENST00000682275.1:c.1253C=
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ENSP00000507852.1:p.Ala418=
|
|
ENST00000683395.1:c.1194C=
|
|
|
ENST00000684087.1:c.1217C=
|
ENSP00000506978.1:p.Ala406=
|
|
ENST00000506362.2:c.968C=
|
ENSP00000424103.2:p.Ala323=
|
|
ENST00000673642.1:c.876C=
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ENSP00000501242.1:p.Cys292=
|
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ENST00000673991.1:c.1253C=
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ENSP00000501033.1:p.Ala418=
|
|
ENST00000226760.5:c.1217C=
MANE Select
|
ENSP00000226760.1:p.Ala406=
|
|
ENST00000503569.5:c.1217C=
|
ENSP00000423337.1:p.Ala406=
|
|
ENST00000507765.1:n.1402C=
|
|
|
NM_001145853.1:c.1217C=
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NP_001139325.1:p.Ala406=
|
|
NM_006005.3:c.1217C=
MANE Select
|
NP_005996.2:p.Ala406=
|
|
XM_017008586.1:c.1226C=
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XP_016864075.1:p.Ala409=
|
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