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ENST00000242839.10:c.2859C=
MANE Select
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XP_011533420.1:n.2730+339C=
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XP_011533421.1:p.Tyr953=
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XP_011533423.1:n.2730+339C=
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XR_941602.1:n.3078C=
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XR_941603.1:n.3078C=
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XR_941604.1:n.3078C=
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NP_001317508.1:p.Tyr869=
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XM_005266431.4:c.2823C=
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XP_006719900.1:p.Tyr921=
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XM_011535117.3:c.2763C=
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XP_011533419.1:p.Tyr921=
|
|
XM_017020627.1:c.2763C=
|
XP_016876116.1:p.Tyr921=
|
|
NM_000053.4:c.2859C=
MANE Select
|
NP_000044.2:p.Tyr953=
|
|
NM_001005918.3:c.2244+339C=
|
NP_001005918.1:n.2244+339C=
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NM_001243182.2:c.2526C=
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NM_001330578.2:c.2625C=
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NP_001317507.1:p.Tyr875=
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