ENST00000262493.12:c.735C>A
MANE Select
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ENSP00000262493.6:p.His245Gln
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ENST00000562316.6:c.402C>A
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ENSP00000457238.2:p.His134Gln
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|
ENST00000564727.2:c.39C>A
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ENSP00000454971.2:p.His13Gln
|
|
ENST00000568375.2:c.116-3471C>A
|
|
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ENST00000638185.1:n.950C>A
|
|
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ENST00000638210.1:n.1035C>A
|
|
|
ENST00000638705.1:c.735C>A
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ENSP00000491223.1:p.His245Gln
|
|
ENST00000638836.1:n.645C>A
|
|
|
ENST00000639055.1:n.1456C>A
|
|
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ENST00000639251.1:n.636C>A
|
|
|
ENST00000639268.1:c.370C>A
|
|
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ENST00000639341.1:c.260C>A
|
|
|
ENST00000639770.1:c.773C>A
|
ENSP00000491999.1:n.773C>A
|
|
ENST00000640390.1:n.665C>A
|
|
|
ENST00000640469.1:c.99C>A
|
ENSP00000491875.1:p.His33Gln
|
|
ENST00000640560.1:n.511C>A
|
|
|
ENST00000640893.1:c.*133C>A
|
ENSP00000492677.1:n.*133C>A
|
|
ENST00000262493.10:c.735C>A
|
ENSP00000262493.6:p.His245Gln
|
|
ENST00000568375.1:n.116-3471C>A
|
|
|
NM_020988.2:c.735C>A
|
NP_066268.1:p.His245Gln
|
|
XM_011523003.1:c.609C>A
|
XP_011521305.1:p.His203Gln
|
|
XM_011523003.3:c.609C>A
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XP_011521305.1:p.His203Gln
|
|
NM_020988.3:c.735C>A
MANE Select
|
NP_066268.1:p.His245Gln
|
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