ENST00000645828.1:n.2755G>T
|
|
|
ENST00000651671.1:c.4948G>T
MANE Select
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ENSP00000498587.1:p.Ala1650Ser
|
|
ENST00000679595.1:c.4948G>T
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ENSP00000506241.1:p.Ala1650Ser
|
|
ENST00000680133.1:c.4834G>T
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ENSP00000505319.1:p.Ala1612Ser
|
|
ENST00000680218.1:c.4828G>T
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ENSP00000505339.1:p.Ala1610Ser
|
|
ENST00000680668.1:c.4834G>T
|
ENSP00000506336.1:p.Ala1612Ser
|
|
ENST00000680778.1:c.2545G>T
|
ENSP00000506033.1:p.Ala849Ser
|
|
ENST00000680924.1:c.*2348G>T
|
ENSP00000506031.1:n.*2348G>T
|
|
ENST00000681135.1:c.*2557G>T
|
ENSP00000506636.1:n.*2557G>T
|
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ENST00000681298.1:n.1761G>T
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|
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ENST00000681454.1:c.*4184G>T
|
ENSP00000505763.1:n.*4184G>T
|
|
ENST00000277541.6:c.4948G>T
|
ENSP00000277541.6:p.Ala1650Ser
|
|
ENST00000494783.1:n.103G>T
|
|
|
NM_017617.3:c.4948G>T
|
NP_060087.3:p.Ala1650Ser
|
|
XM_011518717.1:c.4249G>T
|
XP_011517019.1:p.Ala1417Ser
|
|
NM_017617.5:c.4948G>T
MANE Select
|
NP_060087.3:p.Ala1650Ser
|
|
XM_011518717.2:c.4225G>T
|
XP_011517019.2:p.Ala1409Ser
|
|