ENST00000272286.4:c.1905G>C
MANE Select
|
ENSP00000272286.2:p.Leu635=
|
|
ENST00000272286.2:c.1905G>C
|
ENSP00000272286.2:p.Leu635=
|
|
NM_022437.2:c.1905G>C
|
NP_071882.1:p.Leu635=
|
|
XM_005264483.2:c.1902G>C
|
XP_005264540.1:p.Leu634=
|
|
XM_011533029.1:c.1917G>C
|
XP_011531331.1:p.Leu639=
|
|
XM_011533030.1:c.1914G>C
|
XP_011531332.1:p.Leu638=
|
|
XM_011533031.1:c.1689G>C
|
XP_011531333.1:p.Leu563=
|
|
XR_939707.1:n.2407G>C
|
|
|
NM_001357321.1:c.1902G>C
|
NP_001344250.1:p.Leu634=
|
|
XM_011533029.2:c.1917G>C
|
XP_011531331.1:p.Leu639=
|
|
XM_011533030.2:c.1914G>C
|
XP_011531332.1:p.Leu638=
|
|
XR_001738891.1:n.2421G>C
|
|
|
XR_939707.2:n.2421G>C
|
|
|
NM_022437.3:c.1905G>C
MANE Select
|
NP_071882.1:p.Leu635=
|
|
NM_001357321.2:c.1902G>C
|
NP_001344250.1:p.Leu634=
|
|