ENST00000394867.9:n.1161G>C
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|
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ENST00000687128.1:n.1161G>C
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|
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ENST00000688002.1:n.1016G>C
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|
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ENST00000689792.1:n.646-20G>C
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|
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ENST00000262948.10:c.722G>C
MANE Select
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ENSP00000262948.4:p.Gly241Ala
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ENST00000262948.9:c.722G>C
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ENSP00000262948.3:p.Gly241Ala
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ENST00000394867.8:c.431G>C
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ENSP00000378336.1:p.Gly144Ala
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ENST00000593364.5:n.669G>C
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|
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ENST00000595715.1:n.537G>C
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|
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ENST00000597263.5:n.169+1621G>C
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|
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ENST00000599021.1:c.29+1621G>C
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ENST00000600584.5:n.1282G>C
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|
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ENST00000601786.5:n.1023G>C
|
|
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NM_030662.3:c.722G>C , LRG_750t1:c.722G>C
|
NP_109587.1:p.Gly241Ala
|
|
XM_006722799.2:c.705+1621G>C
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XP_006722862.1:n.705+1621G>C
|
|
XM_011528133.1:c.152G>C
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XP_011526435.1:p.Gly51Ala
|
|
XM_017026989.1:c.722G>C
|
XP_016882478.1:p.Gly241Ala
|
|
XM_017026990.1:c.705+1621G>C
|
XP_016882479.1:n.705+1621G>C
|
|
NM_030662.4:c.722G>C
MANE Select
|
NP_109587.1:p.Gly241Ala
|
|