ENST00000299314.12:c.1028T>C
MANE Select
|
ENSP00000299314.7:p.Val343Ala
|
|
ENST00000299314.11:c.1028T>C
|
ENSP00000299314.7:p.Val343Ala
|
|
ENST00000549940.5:c.1028T>C
|
ENSP00000449150.1:p.Val343Ala
|
|
NM_024312.4:c.1028T>C
|
NP_077288.2:p.Val343Ala
|
|
XM_006719593.2:c.1028T>C
|
XP_006719656.1:p.Val343Ala
|
|
XM_011538731.1:c.947T>C
|
XP_011537033.1:p.Val316Ala
|
|
XM_006719593.3:c.1028T>C
|
XP_006719656.1:p.Val343Ala
|
|
XM_011538731.2:c.947T>C
|
XP_011537033.1:p.Val316Ala
|
|
XM_017019961.1:c.812T>C
|
XP_016875450.1:p.Val271Ala
|
|
XM_017019962.2:c.-200T>C
|
XP_016875451.1:n.-200T>C
|
|
NM_024312.5:c.1028T>C
MANE Select
|
NP_077288.2:p.Val343Ala
|
|