ENST00000238682.8:c.926+402G=
(TGFB3)
MANE Select
|
ENSP00000238682.3:n.926+402G=
|
|
ENST00000556674.2:c.926+402G=
(TGFB3)
|
ENSP00000502685.1:n.926+402G=
|
|
ENST00000238682.7:c.926+402G=
(TGFB3)
|
ENSP00000238682.3:n.926+402G=
|
|
ENST00000554980.5:n.1307+402G=
(TGFB3)
|
|
|
ENST00000555677.5:n.90-25971C=
(IFT43)
|
|
|
ENST00000557493.1:n.392+402G=
(TGFB3)
|
|
|
NM_003239.3:c.926+402G=
(TGFB3)
|
NP_003230.1:n.926+402G=
|
|
XM_005268028.1:c.926+402G=
(TGFB3)
|
XP_005268085.1:n.926+402G=
|
|
NM_001329939.1:c.926+402G=
(TGFB3)
|
NP_001316868.1:n.926+402G=
|
|
NM_003239.4:c.926+402G=
(TGFB3)
|
NP_003230.1:n.926+402G=
|
|
NM_001329939.2:c.926+402G=
(TGFB3)
|
NP_001316868.1:n.926+402G=
|
|
NM_003239.5:c.926+402G=
(TGFB3)
MANE Select
|
NP_003230.1:n.926+402G=
|
|