ENST00000359271.4:c.114T>C
MANE Select
|
ENSP00000352216.2:p.Leu38=
|
|
ENST00000359271.3:c.114T>C
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ENSP00000352216.2:p.Leu38=
|
|
ENST00000611837.1:n.266T>C
|
|
|
NM_030777.3:c.114T>C
|
NP_110404.1:p.Leu38=
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|
XM_011529060.1:c.177T>C
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XP_011527362.1:p.Leu59=
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|
XM_011529061.1:c.123T>C
|
XP_011527363.1:p.Leu41=
|
|
XM_011529062.1:c.177T>C
|
XP_011527364.1:p.Leu59=
|
|
XM_011529063.1:c.177T>C
|
XP_011527365.1:p.Leu59=
|
|
XM_011529064.1:c.177T>C
|
XP_011527366.1:p.Leu59=
|
|
XM_011529065.1:c.177T>C
|
XP_011527367.1:p.Leu59=
|
|
XR_936641.1:n.313T>C
|
|
|
XM_011529060.2:c.177T>C
|
XP_011527362.1:p.Leu59=
|
|
XM_011529061.2:c.123T>C
|
XP_011527363.1:p.Leu41=
|
|
XM_011529062.2:c.177T>C
|
XP_011527364.1:p.Leu59=
|
|
XM_011529063.2:c.177T>C
|
XP_011527365.1:p.Leu59=
|
|
XM_011529064.2:c.177T>C
|
XP_011527366.1:p.Leu59=
|
|
XM_011529065.2:c.177T>C
|
XP_011527367.1:p.Leu59=
|
|
XM_017028087.2:c.114T>C
|
XP_016883576.1:p.Leu38=
|
|
XR_936641.2:n.300T>C
|
|
|
NM_030777.4:c.114T>C
MANE Select
|
NP_110404.1:p.Leu38=
|
|