ENST00000700075.1:c.4C>A
|
ENSP00000514784.1:p.Pro2Thr
|
|
ENST00000342771.10:c.1936C>A
MANE Select
|
ENSP00000344087.4:p.Pro646Thr
|
|
ENST00000439256.2:c.34C>A
|
ENSP00000407058.2:p.Pro12Thr
|
|
ENST00000443672.2:c.271C>A
|
ENSP00000393548.2:p.Pro91Thr
|
|
ENST00000449547.6:c.29C>A
|
|
|
ENST00000464768.2:n.604C>A
|
|
|
ENST00000644359.1:c.517C>A
|
ENSP00000494561.1:p.Pro173Thr
|
|
ENST00000644506.1:c.562C>A
|
ENSP00000496672.1:p.Pro188Thr
|
|
ENST00000644939.1:c.1933C>A
|
ENSP00000496726.1:p.Pro645Thr
|
|
ENST00000644949.1:c.267C>A
|
|
|
ENST00000646136.1:n.247C>A
|
|
|
ENST00000647140.1:c.801C>A
|
|
|
ENST00000342771.8:c.1936C>A
|
ENSP00000344087.4:p.Pro646Thr
|
|
ENST00000406775.6:c.1864C>A
|
ENSP00000385263.2:p.Pro622Thr
|
|
ENST00000439256.1:c.34C>A
|
|
|
ENST00000443672.1:c.516C>A
|
|
|
ENST00000464768.1:n.602C>A
|
|
|
ENST00000465899.1:n.433C>A
|
|
|
ENST00000498384.5:n.304C>A
|
|
|
ENST00000611706.4:c.1192C>A
|
ENSP00000478134.1:p.Pro398Thr
|
|
ENST00000615871.4:c.1120C>A
|
ENSP00000479325.1:p.Pro374Thr
|
|
NM_001127231.2:c.1864C>A
|
NP_001120703.1:p.Pro622Thr
|
|
NM_015570.3:c.1936C>A
|
NP_056385.1:p.Pro646Thr
|
|
XM_005250257.1:c.583C>A
|
XP_005250314.1:p.Pro195Thr
|
|
XM_011516010.1:c.1957C>A
|
XP_011514312.1:p.Pro653Thr
|
|
XM_011516011.1:c.1954C>A
|
XP_011514313.1:p.Pro652Thr
|
|
XM_011516012.1:c.1891C>A
|
XP_011514314.1:p.Pro631Thr
|
|
XM_011516013.1:c.1885C>A
|
XP_011514315.1:p.Pro629Thr
|
|
XM_011516014.1:c.1855C>A
|
XP_011514316.1:p.Pro619Thr
|
|
XM_011516015.1:c.1693C>A
|
XP_011514317.1:p.Pro565Thr
|
|
XM_011516016.1:c.1666C>A
|
XP_011514318.1:p.Pro556Thr
|
|
XM_011516017.1:c.1483C>A
|
XP_011514319.1:p.Pro495Thr
|
|
XM_011516018.1:c.1456C>A
|
XP_011514320.1:p.Pro486Thr
|
|
XM_005250257.2:c.583C>A
|
XP_005250314.1:p.Pro195Thr
|
|
XM_011516010.2:c.1957C>A
|
XP_011514312.1:p.Pro653Thr
|
|
XM_011516011.2:c.1954C>A
|
XP_011514313.1:p.Pro652Thr
|
|
XM_011516012.2:c.1891C>A
|
XP_011514314.1:p.Pro631Thr
|
|
XM_011516013.2:c.1885C>A
|
XP_011514315.1:p.Pro629Thr
|
|
XM_011516014.2:c.1855C>A
|
XP_011514316.1:p.Pro619Thr
|
|
XM_011516017.2:c.1483C>A
|
XP_011514319.1:p.Pro495Thr
|
|
XM_011516018.2:c.1456C>A
|
XP_011514320.1:p.Pro486Thr
|
|
XM_017011951.2:c.1957C>A
|
XP_016867440.1:p.Pro653Thr
|
|
NM_001127231.3:c.1864C>A
|
NP_001120703.1:p.Pro622Thr
|
|
NM_015570.4:c.1936C>A
MANE Select
|
NP_056385.1:p.Pro646Thr
|
|