|
ENST00000328194.8:c.697C>G
MANE Select
|
ENSP00000328524.3:p.Pro233Ala
|
|
|
ENST00000530780.2:c.*523C>G
|
ENSP00000433925.1:n.*523C>G
|
|
|
ENST00000530867.2:n.486C>G
|
|
|
|
ENST00000532696.2:n.620C>G
|
|
|
|
ENST00000679446.1:n.618C>G
|
|
|
|
ENST00000679460.1:n.486C>G
|
|
|
|
ENST00000679568.1:c.697C>G
|
ENSP00000505860.1:p.Pro233Ala
|
|
|
ENST00000679745.1:n.486C>G
|
|
|
|
ENST00000679999.1:c.697C>G
|
ENSP00000505198.1:p.Pro233Ala
|
|
|
ENST00000680252.1:c.486C>G
|
|
|
|
ENST00000680294.1:c.697C>G
|
ENSP00000506113.1:p.Pro233Ala
|
|
|
ENST00000680470.1:c.697C>G
|
ENSP00000505975.1:p.Pro233Ala
|
|
|
ENST00000680554.1:c.409C>G
|
ENSP00000505621.1:p.Pro137Ala
|
|
|
ENST00000680576.1:n.486C>G
|
|
|
|
ENST00000680599.1:n.614C>G
|
|
|
|
ENST00000680742.1:c.697C>G
|
ENSP00000505206.1:p.Pro233Ala
|
|
|
ENST00000680885.1:n.618C>G
|
|
|
|
ENST00000681158.1:c.486C>G
|
|
|
|
ENST00000681173.1:n.486C>G
|
|
|
|
ENST00000681203.1:c.625C>G
|
ENSP00000506456.1:p.Pro209Ala
|
|
|
ENST00000681425.1:n.618C>G
|
|
|
|
ENST00000681915.1:n.486C>G
|
|
|
|
ENST00000328194.7:c.697C>G
|
ENSP00000328524.3:p.Pro233Ala
|
|
|
ENST00000526707.5:c.625C>G
|
ENSP00000436780.1:p.Pro209Ala
|
|
|
ENST00000530044.5:c.697C>G
|
ENSP00000435866.1:p.Pro233Ala
|
|
|
ENST00000532696.1:n.452C>G
|
|
|
|
NM_001243254.1:c.697C>G
|
NP_001230183.1:p.Pro233Ala
|
|
|
NM_015213.3:c.697C>G
|
NP_056028.2:p.Pro233Ala
|
|
|
XM_005252832.1:c.697C>G
|
XP_005252889.1:p.Pro233Ala
|
|
|
XM_011519952.1:c.697C>G
|
XP_011518254.1:p.Pro233Ala
|
|
|
XR_242782.2:n.962C>G
|
|
|
|
XR_930851.1:n.962C>G
|
|
|
|
XR_930852.1:n.962C>G
|
|
|
|
XR_930853.1:n.962C>G
|
|
|
|
NM_001348749.1:c.625C>G
|
NP_001335678.1:p.Pro209Ala
|
|
|
NM_001348750.1:c.409C>G
|
NP_001335679.1:p.Pro137Ala
|
|
|
NR_145966.2:n.954C>G
|
|
|
|
NM_015213.4:c.697C>G
MANE Select
|
NP_056028.2:p.Pro233Ala
|
|
|
NM_001243254.2:c.697C>G
|
NP_001230183.1:p.Pro233Ala
|
|
|
NM_001348749.2:c.625C>G
|
NP_001335678.1:p.Pro209Ala
|
|
|
NM_001348750.2:c.409C>G
|
NP_001335679.1:p.Pro137Ala
|
|
