ENST00000255078.8:c.1491G>T
MANE Select
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ENSP00000255078.4:p.Gly497=
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ENST00000674955.1:c.*208G>T
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ENSP00000502463.1:n.*208G>T
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ENST00000675118.1:c.979G>T
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ENST00000675205.1:n.183+386G>T
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|
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ENST00000675615.1:c.1491G>T
|
ENSP00000502413.1:p.Gly497=
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ENST00000675648.1:n.866G>T
|
|
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ENST00000675997.1:n.113-597G>T
|
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ENST00000676173.1:n.2236G>T
|
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ENST00000676228.1:c.*814G>T
|
ENSP00000502375.1:n.*814G>T
|
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ENST00000255078.7:c.1491G>T
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ENSP00000255078.3:p.Gly497=
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ENST00000537458.5:n.608G>T
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ENST00000539064.5:n.1250G>T
|
|
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ENST00000541229.5:n.186G>T
|
|
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ENST00000543739.5:n.608G>T
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|
|
NM_002180.2:c.1491G>T , LRG_250t1:c.1491G>T
|
NP_002171.2:p.Gly497=
|
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XM_005273974.2:c.480G>T
|
XP_005274031.1:p.Gly160=
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XM_005273975.2:c.363G>T
|
XP_005274032.1:p.Gly121=
|
|
XM_011544994.1:c.258G>T
|
XP_011543296.1:p.Gly86=
|
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XR_949903.1:n.1593G>T
|
|
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XM_005273975.3:c.363G>T
|
XP_005274032.1:p.Gly121=
|
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XM_017017669.2:c.480G>T
|
XP_016873158.1:p.Gly160=
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XM_017017670.2:c.480G>T
|
XP_016873159.1:p.Gly160=
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XM_017017671.2:c.1491G>T
|
XP_016873160.1:p.Gly497=
|
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XR_949903.3:n.1589G>T
|
|
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NM_002180.3:c.1491G>T
MANE Select
|
NP_002171.2:p.Gly497=
|
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