ENST00000272286.4:c.1879G>T
MANE Select
|
ENSP00000272286.2:p.Asp627Tyr
|
|
ENST00000272286.2:c.1879G>T
|
ENSP00000272286.2:p.Asp627Tyr
|
|
NM_022437.2:c.1879G>T
|
NP_071882.1:p.Asp627Tyr
|
|
XM_005264483.2:c.1876G>T
|
XP_005264540.1:p.Asp626Tyr
|
|
XM_011533029.1:c.1891G>T
|
XP_011531331.1:p.Asp631Tyr
|
|
XM_011533030.1:c.1888G>T
|
XP_011531332.1:p.Asp630Tyr
|
|
XM_011533031.1:c.1663G>T
|
XP_011531333.1:p.Asp555Tyr
|
|
XR_939707.1:n.2381G>T
|
|
|
NM_001357321.1:c.1876G>T
|
NP_001344250.1:p.Asp626Tyr
|
|
XM_011533029.2:c.1891G>T
|
XP_011531331.1:p.Asp631Tyr
|
|
XM_011533030.2:c.1888G>T
|
XP_011531332.1:p.Asp630Tyr
|
|
XR_001738891.1:n.2395G>T
|
|
|
XR_939707.2:n.2395G>T
|
|
|
NM_022437.3:c.1879G>T
MANE Select
|
NP_071882.1:p.Asp627Tyr
|
|
NM_001357321.2:c.1876G>T
|
NP_001344250.1:p.Asp626Tyr
|
|