ENST00000362072.8:c.1013C=
MANE Select
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ENSP00000354859.3:p.Ala338=
|
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ENST00000346454.7:c.926C=
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ENSP00000278597.5:p.Ala309=
|
|
ENST00000362072.7:c.1013C=
|
ENSP00000354859.3:p.Ala338=
|
|
ENST00000538967.5:c.1019C=
|
ENSP00000438215.1:p.Ala340=
|
|
ENST00000542968.5:c.1013C=
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ENSP00000442172.1:p.Ala338=
|
|
ENST00000544518.5:c.1010C=
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ENSP00000441068.1:p.Ala337=
|
|
NM_000795.3:c.1013C=
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NP_000786.1:p.Ala338=
|
|
NM_016574.3:c.926C=
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NP_057658.2:p.Ala309=
|
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XM_017017296.2:c.1013C=
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XP_016872785.1:p.Ala338=
|
|
NM_000795.4:c.1013C=
MANE Select
|
NP_000786.1:p.Ala338=
|
|
NM_016574.4:c.926C=
|
NP_057658.2:p.Ala309=
|
|