ENST00000221930.6:c.342G>A
(TGFB1)
MANE Select
|
ENSP00000221930.4:p.Val114=
|
|
ENST00000600196.2:c.342G>A
(TGFB1)
|
ENSP00000504008.1:p.Val114=
|
|
ENST00000677934.1:c.342G>A
(TGFB1)
|
ENSP00000504769.1:p.Val114=
|
|
ENST00000221930.5:c.342G>A
(TGFB1)
|
ENSP00000221930.4:p.Val114=
|
|
ENST00000539627.5:c.-30+1501C>T
(TMEM91)
|
ENSP00000441900.1:n.-30+1501C>T
|
|
ENST00000604424.1:n.350+1501C>T
|
|
|
NM_000660.5:c.342G>A
(TGFB1)
|
NP_000651.3:p.Val114=
|
|
XM_011527242.1:c.342G>A
(TGFB1)
|
XP_011525544.1:p.Val114=
|
|
NM_000660.6:c.342G>A
(TGFB1)
|
NP_000651.3:p.Val114=
|
|
XM_011527242.2:c.342G>A
(TGFB1)
|
XP_011525544.1:p.Val114=
|
|
NM_000660.7:c.342G>A
(TGFB1)
MANE Select
|
NP_000651.3:p.Val114=
|
|