ENST00000700555.2:n.697T>A
|
|
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ENST00000700557.2:n.286T>A
|
|
|
ENST00000700559.2:c.2168-3541T>A
|
ENSP00000515065.2:n.2168-3541T>A
|
|
ENST00000546498.2:n.881T>A
|
|
|
ENST00000549461.2:n.686T>A
|
|
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ENST00000700555.1:c.625T>A
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ENSP00000515062.1:p.Ser209Thr
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|
ENST00000700556.1:c.665T>A
|
|
|
ENST00000700557.1:c.205T>A
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ENSP00000515064.1:p.Ser69Thr
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|
ENST00000700558.1:n.408T>A
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|
|
ENST00000700559.1:c.1383-3541T>A
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|
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ENST00000700560.1:n.1409T>A
|
|
|
ENST00000700561.1:n.1535T>A
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|
|
ENST00000070846.11:c.2326T>A
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ENSP00000070846.6:p.Ser776Thr
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|
ENST00000340811.9:c.2194T>A
MANE Select
|
ENSP00000342800.5:p.Ser732Thr
|
|
ENST00000070846.10:c.2326T>A
|
ENSP00000070846.6:p.Ser776Thr
|
|
ENST00000340811.8:c.2194T>A
|
ENSP00000342800.4:p.Ser732Thr
|
|
ENST00000613243.1:c.2326T>A
|
ENSP00000478295.1:p.Ser776Thr
|
|
NM_001005242.2:c.2194T>A
|
NP_001005242.2:p.Ser732Thr
|
|
NM_004572.3:c.2326T>A , LRG_398t1:c.2326T>A
|
NP_004563.2:p.Ser776Thr
|
|
NM_001005242.3:c.2194T>A
MANE Select
|
NP_001005242.2:p.Ser732Thr
|
|
NM_004572.4:c.2326T>A
|
NP_004563.2:p.Ser776Thr
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