ENST00000700075.1:c.5C>A
|
ENSP00000514784.1:p.Pro2Gln
|
|
ENST00000342771.10:c.1937C>A
MANE Select
|
ENSP00000344087.4:p.Pro646Gln
|
|
ENST00000439256.2:c.35C>A
|
ENSP00000407058.2:p.Pro12Gln
|
|
ENST00000443672.2:c.272C>A
|
ENSP00000393548.2:p.Pro91Gln
|
|
ENST00000449547.6:c.30C>A
|
|
|
ENST00000464768.2:n.605C>A
|
|
|
ENST00000644359.1:c.518C>A
|
ENSP00000494561.1:p.Pro173Gln
|
|
ENST00000644506.1:c.563C>A
|
ENSP00000496672.1:p.Pro188Gln
|
|
ENST00000644939.1:c.1934C>A
|
ENSP00000496726.1:p.Pro645Gln
|
|
ENST00000644949.1:c.268C>A
|
|
|
ENST00000646136.1:n.248C>A
|
|
|
ENST00000647140.1:c.802C>A
|
|
|
ENST00000342771.8:c.1937C>A
|
ENSP00000344087.4:p.Pro646Gln
|
|
ENST00000406775.6:c.1865C>A
|
ENSP00000385263.2:p.Pro622Gln
|
|
ENST00000439256.1:c.35C>A
|
|
|
ENST00000443672.1:c.517C>A
|
|
|
ENST00000464768.1:n.603C>A
|
|
|
ENST00000465899.1:n.434C>A
|
|
|
ENST00000498384.5:n.305C>A
|
|
|
ENST00000611706.4:c.1193C>A
|
ENSP00000478134.1:p.Pro398Gln
|
|
ENST00000615871.4:c.1121C>A
|
ENSP00000479325.1:p.Pro374Gln
|
|
NM_001127231.2:c.1865C>A
|
NP_001120703.1:p.Pro622Gln
|
|
NM_015570.3:c.1937C>A
|
NP_056385.1:p.Pro646Gln
|
|
XM_005250257.1:c.584C>A
|
XP_005250314.1:p.Pro195Gln
|
|
XM_011516010.1:c.1958C>A
|
XP_011514312.1:p.Pro653Gln
|
|
XM_011516011.1:c.1955C>A
|
XP_011514313.1:p.Pro652Gln
|
|
XM_011516012.1:c.1892C>A
|
XP_011514314.1:p.Pro631Gln
|
|
XM_011516013.1:c.1886C>A
|
XP_011514315.1:p.Pro629Gln
|
|
XM_011516014.1:c.1856C>A
|
XP_011514316.1:p.Pro619Gln
|
|
XM_011516015.1:c.1694C>A
|
XP_011514317.1:p.Pro565Gln
|
|
XM_011516016.1:c.1667C>A
|
XP_011514318.1:p.Pro556Gln
|
|
XM_011516017.1:c.1484C>A
|
XP_011514319.1:p.Pro495Gln
|
|
XM_011516018.1:c.1457C>A
|
XP_011514320.1:p.Pro486Gln
|
|
XM_005250257.2:c.584C>A
|
XP_005250314.1:p.Pro195Gln
|
|
XM_011516010.2:c.1958C>A
|
XP_011514312.1:p.Pro653Gln
|
|
XM_011516011.2:c.1955C>A
|
XP_011514313.1:p.Pro652Gln
|
|
XM_011516012.2:c.1892C>A
|
XP_011514314.1:p.Pro631Gln
|
|
XM_011516013.2:c.1886C>A
|
XP_011514315.1:p.Pro629Gln
|
|
XM_011516014.2:c.1856C>A
|
XP_011514316.1:p.Pro619Gln
|
|
XM_011516017.2:c.1484C>A
|
XP_011514319.1:p.Pro495Gln
|
|
XM_011516018.2:c.1457C>A
|
XP_011514320.1:p.Pro486Gln
|
|
XM_017011951.2:c.1958C>A
|
XP_016867440.1:p.Pro653Gln
|
|
NM_001127231.3:c.1865C>A
|
NP_001120703.1:p.Pro622Gln
|
|
NM_015570.4:c.1937C>A
MANE Select
|
NP_056385.1:p.Pro646Gln
|
|