ENST00000262493.12:c.757T>A
MANE Select
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ENSP00000262493.6:p.Ser253Thr
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ENST00000562316.6:c.424T>A
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ENSP00000457238.2:p.Ser142Thr
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ENST00000564727.2:c.61T>A
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ENSP00000454971.2:p.Ser21Thr
|
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ENST00000568375.2:c.116-3449T>A
|
|
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ENST00000638185.1:n.972T>A
|
|
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ENST00000638210.1:n.1057T>A
|
|
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ENST00000638705.1:c.757T>A
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ENSP00000491223.1:p.Ser253Thr
|
|
ENST00000638836.1:n.667T>A
|
|
|
ENST00000639055.1:n.1478T>A
|
|
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ENST00000639251.1:n.658T>A
|
|
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ENST00000639268.1:c.392T>A
|
|
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ENST00000639341.1:c.282T>A
|
|
|
ENST00000639770.1:c.795T>A
|
ENSP00000491999.1:n.795T>A
|
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ENST00000640390.1:n.687T>A
|
|
|
ENST00000640469.1:c.121T>A
|
ENSP00000491875.1:p.Ser41Thr
|
|
ENST00000640560.1:n.533T>A
|
|
|
ENST00000640893.1:c.*155T>A
|
ENSP00000492677.1:n.*155T>A
|
|
ENST00000262493.10:c.757T>A
|
ENSP00000262493.6:p.Ser253Thr
|
|
ENST00000568375.1:n.116-3449T>A
|
|
|
NM_020988.2:c.757T>A
|
NP_066268.1:p.Ser253Thr
|
|
XM_011523003.1:c.631T>A
|
XP_011521305.1:p.Ser211Thr
|
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XM_011523003.3:c.631T>A
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XP_011521305.1:p.Ser211Thr
|
|
NM_020988.3:c.757T>A
MANE Select
|
NP_066268.1:p.Ser253Thr
|
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