ENST00000238682.8:c.831T>C
(TGFB3)
MANE Select
|
ENSP00000238682.3:p.His277=
|
|
ENST00000556674.2:c.831T>C
(TGFB3)
|
ENSP00000502685.1:p.His277=
|
|
ENST00000238682.7:c.831T>C
(TGFB3)
|
ENSP00000238682.3:p.His277=
|
|
ENST00000554980.5:n.1212T>C
(TGFB3)
|
|
|
ENST00000555677.5:n.90-25474A>G
(IFT43)
|
|
|
ENST00000556285.1:c.831T>C
(TGFB3)
|
ENSP00000451110.1:p.His277=
|
|
ENST00000557493.1:n.297T>C
(TGFB3)
|
|
|
NM_003239.3:c.831T>C
(TGFB3)
|
NP_003230.1:p.His277=
|
|
XM_005268028.1:c.831T>C
(TGFB3)
|
XP_005268085.1:p.His277=
|
|
NM_001329938.1:c.831T>C
(TGFB3)
|
NP_001316867.1:p.His277=
|
|
NM_001329939.1:c.831T>C
(TGFB3)
|
NP_001316868.1:p.His277=
|
|
NM_003239.4:c.831T>C
(TGFB3)
|
NP_003230.1:p.His277=
|
|
NM_001329938.2:c.831T>C
(TGFB3)
|
NP_001316867.1:p.His277=
|
|
NM_001329939.2:c.831T>C
(TGFB3)
|
NP_001316868.1:p.His277=
|
|
NM_003239.5:c.831T>C
(TGFB3)
MANE Select
|
NP_003230.1:p.His277=
|
|