ENST00000703637.1:c.351G=
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ENSP00000515413.1:p.Thr117=
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|
ENST00000360864.9:c.351G=
MANE Select
|
ENSP00000354111.4:p.Thr117=
|
|
ENST00000360864.8:c.351G=
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ENSP00000354111.4:p.Thr117=
|
|
ENST00000470551.1:c.351G=
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ENSP00000434744.1:p.Thr117=
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|
NM_025219.2:c.351G=
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NP_079495.1:p.Thr117=
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|
XM_011529048.1:c.351G=
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XP_011527350.1:p.Thr117=
|
|
XM_011529049.1:c.351G=
|
XP_011527351.1:p.Thr117=
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|
XM_011529050.1:c.351G=
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XP_011527352.1:p.Thr117=
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|
XR_936629.1:n.983G=
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|
|
XR_936630.1:n.1241G=
|
|
|
XM_011529048.2:c.351G=
|
XP_011527350.1:p.Thr117=
|
|
XR_936629.2:n.996G=
|
|
|
NM_025219.3:c.351G=
MANE Select
|
NP_079495.1:p.Thr117=
|
|