ENST00000704074.1:c.15G>T
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|
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ENST00000283179.14:c.337G>T
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ENSP00000283179.10:p.Ala113Ser
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ENST00000444376.7:c.337G>T
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ENSP00000393151.2:p.Ala113Ser
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ENST00000476241.2:n.522G>T
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|
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ENST00000638475.1:c.121G>T
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ENSP00000491305.1:p.Ala41Ser
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ENST00000638952.1:n.568G>T
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ENST00000640218.2:c.337G>T
MANE Select
|
ENSP00000491215.1:p.Ala113Ser
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ENST00000640306.1:c.337G>T
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ENSP00000491685.1:p.Ala113Ser
|
|
ENST00000640440.1:c.37G>T
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ENSP00000491263.1:p.Ala13Ser
|
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ENST00000649899.1:n.561G>T
|
|
|
ENST00000283179.13:c.337G>T
|
ENSP00000283179.9:p.Ala113Ser
|
|
ENST00000444376.6:c.337G>T
|
ENSP00000393151.2:p.Ala113Ser
|
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ENST00000476241.1:n.521G>T
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|
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NM_004501.3:c.337G>T
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NP_004492.2:p.Ala113Ser
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NM_031844.2:c.337G>T
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NP_114032.2:p.Ala113Ser
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|
NM_031844.3:c.337G>T
MANE Select
|
NP_114032.2:p.Ala113Ser
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