ENST00000265631.10:c.1744G>T
MANE Select
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ENSP00000265631.6:p.Ala582Ser
|
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ENST00000265631.9:c.1744G>T
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ENSP00000265631.5:p.Ala582Ser
|
|
ENST00000416240.6:c.1747G>T
|
ENSP00000400101.2:p.Ala583Ser
|
|
ENST00000494085.1:n.154G>T
|
|
|
NM_001160210.1:c.1747G>T
|
NP_001153682.1:p.Ala583Ser
|
|
NM_014251.2:c.1744G>T
|
NP_055066.1:p.Ala582Ser
|
|
NR_027662.1:n.1819G>T
|
|
|
XM_006715831.2:c.1777G>T
|
XP_006715894.1:p.Ala593Ser
|
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XM_011515728.1:c.892G>T
|
XP_011514030.1:p.Ala298Ser
|
|
XM_006715831.4:c.1777G>T
|
XP_006715894.1:p.Ala593Ser
|
|
XM_017011663.1:c.1735G>T
|
XP_016867152.1:p.Ala579Ser
|
|
XM_017011664.2:c.892G>T
|
XP_016867153.1:p.Ala298Ser
|
|
XM_017011665.1:c.892G>T
|
XP_016867154.1:p.Ala298Ser
|
|
XR_001744525.2:n.1990G>T
|
|
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XR_002956405.1:n.2548G>T
|
|
|
NM_014251.3:c.1744G>T
MANE Select
|
NP_055066.1:p.Ala582Ser
|
|
NR_027662.2:n.1770G>T
|
|
|
NM_001160210.2:c.1747G>T
|
NP_001153682.1:p.Ala583Ser
|
|