ENST00000706989.1:c.2045C>A
|
ENSP00000516702.1:p.Pro682Gln
|
|
ENST00000359125.7:c.1991C>A
MANE Select
|
ENSP00000352035.2:p.Pro664Gln
|
|
ENST00000637193.1:c.1388C>A
|
ENSP00000490734.1:p.Pro463Gln
|
|
ENST00000344462.8:c.1898C>A
|
ENSP00000339611.4:p.Pro633Gln
|
|
ENST00000357249.6:c.1559C>A
|
ENSP00000349789.3:p.Pro520Gln
|
|
ENST00000359125.6:c.1991C>A
|
ENSP00000352035.2:p.Pro664Gln
|
|
ENST00000360480.7:c.1907C>A
|
ENSP00000353668.3:p.Pro636Gln
|
|
ENST00000370224.5:c.2015C>A
|
ENSP00000359244.2:p.Pro672Gln
|
|
ENST00000625514.2:c.1979C>A
|
ENSP00000486040.1:p.Pro660Gln
|
|
ENST00000626839.2:c.1937C>A
|
ENSP00000486706.1:p.Pro646Gln
|
|
ENST00000629241.2:c.1907C>A
|
ENSP00000487142.1:p.Pro636Gln
|
|
ENST00000629676.2:c.1679+6178C>A
|
ENSP00000486194.1:n.1679+6178C>A
|
|
NM_004518.4:c.1907C>A
|
NP_004509.2:p.Pro636Gln
|
|
NM_172106.1:c.1937C>A
|
NP_742104.1:p.Pro646Gln
|
|
NM_172107.2:c.1991C>A
|
NP_742105.1:p.Pro664Gln
|
|
NM_172108.3:c.1898C>A
|
NP_742106.1:p.Pro633Gln
|
|
XM_006723787.1:c.2033C>A
|
XP_006723850.1:p.Pro678Gln
|
|
XM_011528807.1:c.2099C>A
|
XP_011527109.1:p.Pro700Gln
|
|
XM_011528808.1:c.2096C>A
|
XP_011527110.1:p.Pro699Gln
|
|
XM_011528809.1:c.2069C>A
|
XP_011527111.1:p.Pro690Gln
|
|
XM_011528810.1:c.2045C>A
|
XP_011527112.1:p.Pro682Gln
|
|
XM_011528811.1:c.2015C>A
|
XP_011527113.1:p.Pro672Gln
|
|
XM_011528812.1:c.1988C>A
|
XP_011527114.1:p.Pro663Gln
|
|
XM_011528813.1:c.1973C>A
|
XP_011527115.1:p.Pro658Gln
|
|
XM_011528814.1:c.1580C>A
|
XP_011527116.1:p.Pro527Gln
|
|
NM_004518.5:c.1907C>A
|
NP_004509.2:p.Pro636Gln
|
|
NM_172106.2:c.1937C>A
|
NP_742104.1:p.Pro646Gln
|
|
NM_172107.3:c.1991C>A
|
NP_742105.1:p.Pro664Gln
|
|
NM_172108.4:c.1898C>A
|
NP_742106.1:p.Pro633Gln
|
|
XM_011528810.2:c.2045C>A
|
XP_011527112.1:p.Pro682Gln
|
|
XM_011528811.2:c.2015C>A
|
XP_011527113.1:p.Pro672Gln
|
|
XM_017027841.2:c.2042C>A
|
XP_016883330.1:p.Pro681Gln
|
|
XM_017027842.2:c.1979C>A
|
XP_016883331.1:p.Pro660Gln
|
|
XM_017027843.1:c.1976C>A
|
XP_016883332.1:p.Pro659Gln
|
|
XM_017027844.2:c.1934C>A
|
XP_016883333.1:p.Pro645Gln
|
|
XM_017027845.1:c.1007C>A
|
XP_016883334.1:p.Pro336Gln
|
|
NM_004518.6:c.1907C>A
|
NP_004509.2:p.Pro636Gln
|
|
NM_172106.3:c.1937C>A
|
NP_742104.1:p.Pro646Gln
|
|
NM_172107.4:c.1991C>A
MANE Select
|
NP_742105.1:p.Pro664Gln
|
|
NM_172108.5:c.1898C>A
|
NP_742106.1:p.Pro633Gln
|
|
NM_001382235.1:c.2045C>A
|
NP_001369164.1:p.Pro682Gln
|
|