ENST00000305877.13:c.2300T>C
MANE Select
|
ENSP00000303507.8:p.Val767Ala
|
|
ENST00000305877.12:c.2300T>C
|
ENSP00000303507.8:p.Val767Ala
|
|
ENST00000359540.7:c.2300T>C
|
ENSP00000352535.3:p.Val767Ala
|
|
ENST00000398512.9:c.1270-3049T>C
|
ENSP00000381524.6:n.1270-3049T>C
|
|
ENST00000427791.1:c.752T>C
|
ENSP00000396531.1:p.Val251Ala
|
|
ENST00000466076.1:n.374T>C
|
|
|
ENST00000487968.5:n.953T>C
|
|
|
NM_004327.3:c.2300T>C
|
NP_004318.3:p.Val767Ala
|
|
NM_021574.2:c.2300T>C
|
NP_067585.2:p.Val767Ala
|
|
NM_004327.4:c.2300T>C
MANE Select
|
NP_004318.3:p.Val767Ala
|
|
NM_021574.3:c.2300T>C
|
NP_067585.2:p.Val767Ala
|
|