ENST00000706989.1:c.2178C>A
|
ENSP00000516702.1:p.Pro726=
|
|
ENST00000359125.7:c.2124C>A
MANE Select
|
ENSP00000352035.2:p.Pro708=
|
|
ENST00000637193.1:c.1521C>A
|
ENSP00000490734.1:p.Pro507=
|
|
ENST00000344462.8:c.2031C>A
|
ENSP00000339611.4:p.Pro677=
|
|
ENST00000357249.6:c.1692C>A
|
ENSP00000349789.3:p.Pro564=
|
|
ENST00000359125.6:c.2124C>A
|
ENSP00000352035.2:p.Pro708=
|
|
ENST00000360480.7:c.2040C>A
|
ENSP00000353668.3:p.Pro680=
|
|
ENST00000370224.5:c.2148C>A
|
ENSP00000359244.2:p.Pro716=
|
|
ENST00000625514.2:c.2112C>A
|
ENSP00000486040.1:p.Pro704=
|
|
ENST00000626839.2:c.2070C>A
|
ENSP00000486706.1:p.Pro690=
|
|
ENST00000629241.2:c.2040C>A
|
ENSP00000487142.1:p.Pro680=
|
|
ENST00000629676.2:c.1680-6296C>A
|
ENSP00000486194.1:n.1680-6296C>A
|
|
NM_004518.4:c.2040C>A
|
NP_004509.2:p.Pro680=
|
|
NM_172106.1:c.2070C>A
|
NP_742104.1:p.Pro690=
|
|
NM_172107.2:c.2124C>A
|
NP_742105.1:p.Pro708=
|
|
NM_172108.3:c.2031C>A
|
NP_742106.1:p.Pro677=
|
|
XM_006723787.1:c.2166C>A
|
XP_006723850.1:p.Pro722=
|
|
XM_011528807.1:c.2232C>A
|
XP_011527109.1:p.Pro744=
|
|
XM_011528808.1:c.2229C>A
|
XP_011527110.1:p.Pro743=
|
|
XM_011528809.1:c.2202C>A
|
XP_011527111.1:p.Pro734=
|
|
XM_011528810.1:c.2178C>A
|
XP_011527112.1:p.Pro726=
|
|
XM_011528811.1:c.2148C>A
|
XP_011527113.1:p.Pro716=
|
|
XM_011528812.1:c.2121C>A
|
XP_011527114.1:p.Pro707=
|
|
XM_011528813.1:c.2106C>A
|
XP_011527115.1:p.Pro702=
|
|
XM_011528814.1:c.1713C>A
|
XP_011527116.1:p.Pro571=
|
|
NM_004518.5:c.2040C>A
|
NP_004509.2:p.Pro680=
|
|
NM_172106.2:c.2070C>A
|
NP_742104.1:p.Pro690=
|
|
NM_172107.3:c.2124C>A
|
NP_742105.1:p.Pro708=
|
|
NM_172108.4:c.2031C>A
|
NP_742106.1:p.Pro677=
|
|
XM_011528810.2:c.2178C>A
|
XP_011527112.1:p.Pro726=
|
|
XM_011528811.2:c.2148C>A
|
XP_011527113.1:p.Pro716=
|
|
XM_017027841.2:c.2175C>A
|
XP_016883330.1:p.Pro725=
|
|
XM_017027842.2:c.2112C>A
|
XP_016883331.1:p.Pro704=
|
|
XM_017027843.1:c.2109C>A
|
XP_016883332.1:p.Pro703=
|
|
XM_017027844.2:c.2067C>A
|
XP_016883333.1:p.Pro689=
|
|
XM_017027845.1:c.1140C>A
|
XP_016883334.1:p.Pro380=
|
|
NM_004518.6:c.2040C>A
|
NP_004509.2:p.Pro680=
|
|
NM_172106.3:c.2070C>A
|
NP_742104.1:p.Pro690=
|
|
NM_172107.4:c.2124C>A
MANE Select
|
NP_742105.1:p.Pro708=
|
|
NM_172108.5:c.2031C>A
|
NP_742106.1:p.Pro677=
|
|
NM_001382235.1:c.2178C>A
|
NP_001369164.1:p.Pro726=
|
|