ENST00000289473.11:c.1107G>C
MANE Select
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ENSP00000289473.4:p.Pro369=
|
|
ENST00000289473.10:c.1107G>C
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ENSP00000289473.4:p.Pro369=
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|
ENST00000289473.8:c.1107G>C
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ENSP00000289473.4:p.Pro369=
|
|
ENST00000398421.6:n.2134G>C
|
|
|
ENST00000455062.2:n.1216G>C
|
|
|
NM_000265.5:c.1107G>C
|
NP_000256.4:p.Pro369=
|
|
XM_005250543.3:c.*28G>C
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XP_005250600.2:n.*28G>C
|
|
XM_011516498.1:c.1106G>C
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XP_011514800.1:p.Arg369Pro
|
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XM_011516501.1:c.714G>C
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XP_011514803.1:p.Pro238=
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|
NM_000265.6:c.1107G>C
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NP_000256.4:p.Pro369=
|
|
NM_000265.7:c.1107G>C
MANE Select
|
NP_000256.4:p.Pro369=
|
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