ENST00000375128.5:c.698G>C
MANE Select
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ENSP00000364270.5:p.Ser233Thr
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ENST00000375128.4:c.698G>C
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ENSP00000364270.4:p.Ser233Thr
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|
ENST00000462523.5:c.*134G>C
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ENSP00000433006.1:n.*134G>C
|
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ENST00000485042.1:n.210G>C
|
|
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NM_000380.3:c.698G>C , LRG_471t1:c.698G>C
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NP_000371.1:p.Ser233Thr
|
|
NR_027302.1:n.1046G>C
|
|
|
XM_006717278.1:c.698G>C
|
XP_006717341.1:p.Ser233Thr
|
|
XM_011518988.1:c.698G>C
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XP_011517290.1:p.Ser233Thr
|
|
XR_929839.1:n.1229G>C
|
|
|
NM_001354975.1:c.572G>C
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NP_001341904.1:p.Ser191Thr
|
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NR_149091.1:n.543G>C
|
|
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NR_149092.1:n.709G>C
|
|
|
NR_149093.1:n.1235G>C
|
|
|
NR_149094.1:n.1129G>C
|
|
|
NM_000380.4:c.698G>C
MANE Select
|
NP_000371.1:p.Ser233Thr
|
|
NM_001354975.2:c.572G>C
|
NP_001341904.1:p.Ser191Thr
|
|
NR_027302.2:n.977G>C
|
|
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NR_149091.2:n.474G>C
|
|
|
NR_149092.2:n.640G>C
|
|
|
NR_149093.2:n.1166G>C
|
|
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NR_149094.2:n.1060G>C
|
|
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