ENST00000260943.11:c.1325T>C
|
ENSP00000260943.7:p.Ile442Thr
|
|
ENST00000342788.9:c.1325T>C
MANE Select
|
ENSP00000342235.4:p.Ile442Thr
|
|
ENST00000402597.6:c.1247T>C
|
ENSP00000385565.3:p.Ile416Thr
|
|
ENST00000260943.10:c.1324T>C
|
|
|
ENST00000342788.8:c.1325T>C
|
ENSP00000342235.4:p.Ile442Thr
|
|
ENST00000402597.5:c.1148T>C
|
ENSP00000385565.2:p.Ile383Thr
|
|
ENST00000436443.5:c.1325T>C
|
ENSP00000403204.1:p.Ile442Thr
|
|
ENST00000484594.5:n.1377T>C
|
|
|
NM_001042599.1:c.1325T>C
|
NP_001036064.1:p.Ile442Thr
|
|
NM_005235.2:c.1325T>C
|
NP_005226.1:p.Ile442Thr
|
|
XM_005246375.1:c.1325T>C
|
XP_005246432.1:p.Ile442Thr
|
|
XM_005246376.1:c.1325T>C
|
XP_005246433.1:p.Ile442Thr
|
|
XM_005246377.1:c.1325T>C
|
XP_005246434.1:p.Ile442Thr
|
|
XM_006712364.1:c.1325T>C
|
XP_006712427.1:p.Ile442Thr
|
|
XM_005246376.3:c.1325T>C
|
XP_005246433.1:p.Ile442Thr
|
|
XM_005246377.3:c.1325T>C
|
XP_005246434.1:p.Ile442Thr
|
|
XM_006712364.3:c.1325T>C
|
XP_006712427.1:p.Ile442Thr
|
|
XM_017003577.2:c.1403T>C
|
XP_016859066.1:p.Ile468Thr
|
|
XM_017003578.2:c.1403T>C
|
XP_016859067.1:p.Ile468Thr
|
|
XM_017003579.2:c.1403T>C
|
XP_016859068.1:p.Ile468Thr
|
|
XM_017003580.2:c.1403T>C
|
XP_016859069.1:p.Ile468Thr
|
|
XM_017003581.2:c.1403T>C
|
XP_016859070.1:p.Ile468Thr
|
|
XM_017003582.1:c.704T>C
|
XP_016859071.1:p.Ile235Thr
|
|
NM_005235.3:c.1325T>C
MANE Select
|
NP_005226.1:p.Ile442Thr
|
|