ENST00000593677.2:c.1142G>C
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|
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ENST00000688602.1:c.2539G>C
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|
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ENST00000689936.1:c.2511G>C
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|
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ENST00000359596.8:c.14206G>C
MANE Select
|
ENSP00000352608.2:p.Glu4736Gln
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ENST00000355481.8:c.14191G>C
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ENSP00000347667.3:p.Glu4731Gln
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|
ENST00000359596.7:c.14206G>C
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ENSP00000352608.2:p.Glu4736Gln
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ENST00000360985.7:c.14188G>C
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ENSP00000354254.4:p.Glu4730Gln
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NM_000540.2:c.14206G>C , LRG_766t1:c.14206G>C
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NP_000531.2:p.Glu4736Gln
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NM_001042723.1:c.14191G>C
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NP_001036188.1:p.Glu4731Gln
|
|
XM_006723317.1:c.14188G>C
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XP_006723380.1:p.Glu4730Gln
|
|
XM_006723319.1:c.14173G>C
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XP_006723382.1:p.Glu4725Gln
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|
XM_011527204.1:c.14203G>C
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XP_011525506.1:p.Glu4735Gln
|
|
XM_011527205.1:c.14119G>C
|
XP_011525507.1:p.Glu4707Gln
|
|
XM_006723317.2:c.14188G>C
|
XP_006723380.1:p.Glu4730Gln
|
|
XM_006723319.2:c.14173G>C
|
XP_006723382.1:p.Glu4725Gln
|
|
XM_011527205.2:c.14119G>C
|
XP_011525507.1:p.Glu4707Gln
|
|
NM_000540.3:c.14206G>C
MANE Select
|
NP_000531.2:p.Glu4736Gln
|
|
NM_001042723.2:c.14191G>C
|
NP_001036188.1:p.Glu4731Gln
|
|