ENST00000297289.9:c.980T>C
|
ENSP00000516619.1:p.Val327Ala
|
|
ENST00000418964.2:c.2078T>C
|
ENSP00000389424.2:p.Val693Ala
|
|
ENST00000706906.1:c.*2047T>C
|
ENSP00000516618.1:n.*2047T>C
|
|
ENST00000308192.14:c.2027T>C
MANE Select
|
ENSP00000308938.9:p.Val676Ala
|
|
ENST00000308192.13:c.2027T>C
|
ENSP00000308938.9:p.Val676Ala
|
|
ENST00000461414.2:n.50T>C
|
|
|
ENST00000467466.1:n.328T>C
|
|
|
NM_000301.3:c.2027T>C , LRG_571t1:c.2027T>C
|
NP_000292.1:p.Val676Ala
|
|
NM_000301.4:c.2027T>C
|
NP_000292.1:p.Val676Ala
|
|
NM_000301.5:c.2027T>C
MANE Select
|
NP_000292.1:p.Val676Ala
|
|