ENST00000534624.6:c.1444G>T
MANE Select
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ENSP00000432083.1:p.Ala482Ser
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ENST00000227378.7:c.1444G>T
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ENSP00000227378.3:p.Ala482Ser
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|
ENST00000453788.6:c.1387+57G>T
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ENSP00000404372.2:n.1387+57G>T
|
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ENST00000524552.5:c.217G>T
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ENSP00000435908.1:p.Ala73Ser
|
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ENST00000526110.5:c.1387G>T
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ENSP00000433584.1:p.Ala463Ser
|
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ENST00000526686.1:c.100G>T
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ENSP00000435019.1:p.Ala34Ser
|
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ENST00000532091.1:n.1419G>T
|
|
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ENST00000532636.5:c.1444G>T
|
ENSP00000437125.1:p.Ala482Ser
|
|
ENST00000533540.5:c.1006G>T
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ENSP00000437189.1:p.Ala336Ser
|
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ENST00000534319.5:c.736G>T
|
ENSP00000433316.1:p.Ala246Ser
|
|
ENST00000534624.5:c.1444G>T
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ENSP00000432083.1:p.Ala482Ser
|
|
NM_006597.5:c.1444G>T
|
NP_006588.1:p.Ala482Ser
|
|
NM_153201.3:c.1387+57G>T
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NP_694881.1:n.1387+57G>T
|
|
XM_011542798.1:c.1444G>T
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XP_011541100.1:p.Ala482Ser
|
|
NM_006597.6:c.1444G>T
MANE Select
|
NP_006588.1:p.Ala482Ser
|
|
NM_153201.4:c.1387+57G>T
|
NP_694881.1:n.1387+57G>T
|
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