ENST00000324001.8:c.2088G>T
MANE Select
|
ENSP00000326018.6:p.Val696=
|
|
ENST00000673881.1:c.1671G>T
|
ENSP00000501070.1:p.Val557=
|
|
ENST00000674005.2:c.2373G>T
|
ENSP00000501261.1:p.Val791=
|
|
ENST00000674773.1:c.1671G>T
|
ENSP00000502579.1:p.Val557=
|
|
ENST00000675517.1:c.1963G>T
|
|
|
ENST00000676076.1:c.1949G>T
|
|
|
ENST00000676260.1:c.2050G>T
|
|
|
ENST00000676316.1:c.1975G>T
|
|
|
ENST00000291825.11:c.*2293G>T
|
ENSP00000291825.6:n.*2293G>T
|
|
ENST00000324001.7:c.2088G>T
|
ENSP00000326018.6:p.Val696=
|
|
NM_020956.2:c.*2293G>T , LRG_265t1:c.*2293G>T
|
NP_066007.1:n.*2293G>T
|
|
NM_181882.2:c.2088G>T , LRG_265t2:c.2088G>T
|
NP_870998.2:p.Val696=
|
|
XM_011527171.1:c.2088G>T
|
XP_011525473.1:p.Val696=
|
|
XM_011527171.2:c.2088G>T
|
XP_011525473.1:p.Val696=
|
|
XM_017027046.1:c.1986G>T
|
XP_016882535.1:p.Val662=
|
|
XM_017027047.1:c.1986G>T
|
XP_016882536.1:p.Val662=
|
|
NM_181882.3:c.2088G>T
MANE Select
|
NP_870998.2:p.Val696=
|
|