ENST00000254108.12:c.895G>C
MANE Select
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ENSP00000254108.8:p.Glu299Gln
|
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ENST00000254108.11:c.895G>C
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ENSP00000254108.7:p.Glu299Gln
|
|
ENST00000380244.7:c.892G>C
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ENSP00000369594.3:p.Glu298Gln
|
|
ENST00000474990.5:n.189G>C
|
|
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ENST00000487509.6:n.4070G>C
|
|
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ENST00000564766.1:n.719G>C
|
|
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ENST00000566605.5:c.*68G>C
|
ENSP00000455073.1:n.*68G>C
|
|
ENST00000568685.1:c.898G>C
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ENSP00000455282.1:p.Glu300Gln
|
|
ENST00000568901.2:n.269G>C
|
|
|
NM_001170634.1:c.892G>C
|
NP_001164105.1:p.Glu298Gln
|
|
NM_001170937.1:c.883G>C
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NP_001164408.1:p.Glu295Gln
|
|
NM_004960.3:c.895G>C , LRG_655t1:c.895G>C
|
NP_004951.1:p.Glu299Gln
|
|
NR_028388.2:n.965G>C
|
|
|
XM_005255233.3:c.280G>C
|
XP_005255290.1:p.Glu94Gln
|
|
XM_011545781.1:c.889G>C
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XP_011544083.1:p.Glu297Gln
|
|
XM_011545782.1:c.280G>C
|
XP_011544084.1:p.Glu94Gln
|
|
XM_005255233.5:c.280G>C
|
XP_005255290.1:p.Glu94Gln
|
|
XM_011545782.2:c.280G>C
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XP_011544084.1:p.Glu94Gln
|
|
XM_024450221.1:c.886G>C
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XP_024305989.1:p.Glu296Gln
|
|
NM_004960.4:c.895G>C
MANE Select
|
NP_004951.1:p.Glu299Gln
|
|