ENST00000593677.2:c.1538G>C
|
|
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ENST00000688602.1:c.2935G>C
|
|
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ENST00000689936.1:c.2907G>C
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|
|
ENST00000359596.8:c.14602G>C
MANE Select
|
ENSP00000352608.2:p.Glu4868Gln
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|
ENST00000355481.8:c.14587G>C
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ENSP00000347667.3:p.Glu4863Gln
|
|
ENST00000359596.7:c.14602G>C
|
ENSP00000352608.2:p.Glu4868Gln
|
|
ENST00000360985.7:c.14584G>C
|
ENSP00000354254.4:p.Glu4862Gln
|
|
NM_000540.2:c.14602G>C , LRG_766t1:c.14602G>C
|
NP_000531.2:p.Glu4868Gln
|
|
NM_001042723.1:c.14587G>C
|
NP_001036188.1:p.Glu4863Gln
|
|
XM_006723317.1:c.14584G>C
|
XP_006723380.1:p.Glu4862Gln
|
|
XM_006723319.1:c.14569G>C
|
XP_006723382.1:p.Glu4857Gln
|
|
XM_011527204.1:c.14599G>C
|
XP_011525506.1:p.Glu4867Gln
|
|
XM_011527205.1:c.14515G>C
|
XP_011525507.1:p.Glu4839Gln
|
|
XM_006723317.2:c.14584G>C
|
XP_006723380.1:p.Glu4862Gln
|
|
XM_006723319.2:c.14569G>C
|
XP_006723382.1:p.Glu4857Gln
|
|
XM_011527205.2:c.14515G>C
|
XP_011525507.1:p.Glu4839Gln
|
|
NM_000540.3:c.14602G>C
MANE Select
|
NP_000531.2:p.Glu4868Gln
|
|
NM_001042723.2:c.14587G>C
|
NP_001036188.1:p.Glu4863Gln
|
|