ENST00000324001.8:c.2301T>A
MANE Select
|
ENSP00000326018.6:p.His767Gln
|
|
ENST00000673881.1:c.1884T>A
|
ENSP00000501070.1:p.His628Gln
|
|
ENST00000674005.2:c.2586T>A
|
ENSP00000501261.1:p.His862Gln
|
|
ENST00000674773.1:c.1884T>A
|
ENSP00000502579.1:p.His628Gln
|
|
ENST00000675517.1:c.2176T>A
|
|
|
ENST00000676076.1:c.2162T>A
|
|
|
ENST00000676260.1:c.2263T>A
|
|
|
ENST00000676316.1:c.2188T>A
|
|
|
ENST00000291825.11:c.*2506T>A
|
ENSP00000291825.6:n.*2506T>A
|
|
ENST00000324001.7:c.2301T>A
|
ENSP00000326018.6:p.His767Gln
|
|
NM_020956.2:c.*2506T>A , LRG_265t1:c.*2506T>A
|
NP_066007.1:n.*2506T>A
|
|
NM_181882.2:c.2301T>A , LRG_265t2:c.2301T>A
|
NP_870998.2:p.His767Gln
|
|
XM_011527171.1:c.2301T>A
|
XP_011525473.1:p.His767Gln
|
|
XM_011527171.2:c.2301T>A
|
XP_011525473.1:p.His767Gln
|
|
XM_017027046.1:c.2199T>A
|
XP_016882535.1:p.His733Gln
|
|
XM_017027047.1:c.2199T>A
|
XP_016882536.1:p.His733Gln
|
|
NM_181882.3:c.2301T>A
MANE Select
|
NP_870998.2:p.His767Gln
|
|