ENST00000348729.8:c.779C=
MANE Select
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ENSP00000302701.4:p.Ala260=
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ENST00000348729.7:c.779C=
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ENSP00000302701.4:p.Ala260=
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|
ENST00000353963.7:c.791C=
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ENSP00000302851.5:p.Ala264=
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ENST00000504513.1:c.164+132C=
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|
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ENST00000506512.1:n.390C=
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|
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NM_005847.4:c.779C=
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NP_005838.3:p.Ala260=
|
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NM_152685.3:c.791C=
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NP_689898.2:p.Ala264=
|
|
XM_005272148.3:c.899C=
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XP_005272205.3:p.Ala300=
|
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XM_005272149.3:c.887C=
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XP_005272206.3:p.Ala296=
|
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XM_006714741.2:c.899C=
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XP_006714804.2:p.Ala300=
|
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XM_011543765.1:c.899C=
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XP_011542067.1:p.Ala300=
|
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XM_011543766.1:c.680C=
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XP_011542068.1:p.Ala227=
|
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XM_011543767.1:c.584C=
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XP_011542069.1:p.Ala195=
|
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XM_011543768.1:c.464C=
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XP_011542070.1:p.Ala155=
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XM_011543769.1:c.74C=
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XP_011542071.1:p.Ala25=
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XM_005272149.4:c.887C=
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XP_005272206.3:p.Ala296=
|
|
XM_011543765.2:c.899C=
|
XP_011542067.1:p.Ala300=
|
|
NM_005847.5:c.779C=
MANE Select
|
NP_005838.3:p.Ala260=
|
|
NM_152685.4:c.791C=
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NP_689898.2:p.Ala264=
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