ENST00000560968.6:c.690G>A
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ENSP00000453965.2:p.Glu230=
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ENST00000257555.11:c.690G>A
MANE Select
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ENSP00000257555.5:p.Glu230=
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ENST00000257555.10:c.690G>A
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ENSP00000257555.4:p.Glu230=
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ENST00000400024.6:c.690G>A
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ENSP00000476181.1:p.Glu230=
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ENST00000402929.5:n.825G>A
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|
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ENST00000535955.5:n.43-3808G>A
|
|
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ENST00000538626.2:n.191-3808G>A
|
|
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ENST00000538646.5:c.527-481G>A
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ENSP00000443964.1:n.527-481G>A
|
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ENST00000540108.1:c.*130G>A
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ENSP00000445445.1:n.*130G>A
|
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ENST00000541395.5:c.690G>A
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ENSP00000443112.1:p.Glu230=
|
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ENST00000541924.5:c.690G>A
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ENSP00000440361.1:p.Glu230=
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ENST00000543427.5:c.633+57G>A
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ENSP00000439721.2:n.633+57G>A
|
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ENST00000544413.2:c.690G>A
|
ENSP00000438804.1:p.Glu230=
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ENST00000544574.5:c.73-2934G>A
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ENSP00000438565.1:n.73-2934G>A
|
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ENST00000560968.5:c.833G>A
|
|
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ENST00000615446.4:c.-257-2579G>A
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ENSP00000483994.1:n.-257-2579G>A
|
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ENST00000617366.4:c.586+104G>A
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ENSP00000481967.1:n.586+104G>A
|
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NM_000545.5:c.690G>A , LRG_522t1:c.690G>A
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NP_000536.5:p.Glu230=
|
|
NM_000545.6:c.690G>A
|
NP_000536.5:p.Glu230=
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NM_001306179.1:c.690G>A
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NP_001293108.1:p.Glu230=
|
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XM_005253931.2:c.690G>A
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XP_005253988.1:p.Glu230=
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XM_024449168.1:c.690G>A
|
XP_024304936.1:p.Glu230=
|
|
NM_000545.8:c.690G>A
MANE Select
|
NP_000536.6:p.Glu230=
|
|
NM_001306179.2:c.690G>A
|
NP_001293108.2:p.Glu230=
|
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