ENST00000706989.1:c.2044C>T
|
ENSP00000516702.1:p.Pro682Ser
|
|
ENST00000359125.7:c.1990C>T
MANE Select
|
ENSP00000352035.2:p.Pro664Ser
|
|
ENST00000637193.1:c.1387C>T
|
ENSP00000490734.1:p.Pro463Ser
|
|
ENST00000344462.8:c.1897C>T
|
ENSP00000339611.4:p.Pro633Ser
|
|
ENST00000357249.6:c.1558C>T
|
ENSP00000349789.3:p.Pro520Ser
|
|
ENST00000359125.6:c.1990C>T
|
ENSP00000352035.2:p.Pro664Ser
|
|
ENST00000360480.7:c.1906C>T
|
ENSP00000353668.3:p.Pro636Ser
|
|
ENST00000370224.5:c.2014C>T
|
ENSP00000359244.2:p.Pro672Ser
|
|
ENST00000625514.2:c.1978C>T
|
ENSP00000486040.1:p.Pro660Ser
|
|
ENST00000626839.2:c.1936C>T
|
ENSP00000486706.1:p.Pro646Ser
|
|
ENST00000629241.2:c.1906C>T
|
ENSP00000487142.1:p.Pro636Ser
|
|
ENST00000629676.2:c.1679+6177C>T
|
ENSP00000486194.1:n.1679+6177C>T
|
|
NM_004518.4:c.1906C>T
|
NP_004509.2:p.Pro636Ser
|
|
NM_172106.1:c.1936C>T
|
NP_742104.1:p.Pro646Ser
|
|
NM_172107.2:c.1990C>T
|
NP_742105.1:p.Pro664Ser
|
|
NM_172108.3:c.1897C>T
|
NP_742106.1:p.Pro633Ser
|
|
XM_006723787.1:c.2032C>T
|
XP_006723850.1:p.Pro678Ser
|
|
XM_011528807.1:c.2098C>T
|
XP_011527109.1:p.Pro700Ser
|
|
XM_011528808.1:c.2095C>T
|
XP_011527110.1:p.Pro699Ser
|
|
XM_011528809.1:c.2068C>T
|
XP_011527111.1:p.Pro690Ser
|
|
XM_011528810.1:c.2044C>T
|
XP_011527112.1:p.Pro682Ser
|
|
XM_011528811.1:c.2014C>T
|
XP_011527113.1:p.Pro672Ser
|
|
XM_011528812.1:c.1987C>T
|
XP_011527114.1:p.Pro663Ser
|
|
XM_011528813.1:c.1972C>T
|
XP_011527115.1:p.Pro658Ser
|
|
XM_011528814.1:c.1579C>T
|
XP_011527116.1:p.Pro527Ser
|
|
NM_004518.5:c.1906C>T
|
NP_004509.2:p.Pro636Ser
|
|
NM_172106.2:c.1936C>T
|
NP_742104.1:p.Pro646Ser
|
|
NM_172107.3:c.1990C>T
|
NP_742105.1:p.Pro664Ser
|
|
NM_172108.4:c.1897C>T
|
NP_742106.1:p.Pro633Ser
|
|
XM_011528810.2:c.2044C>T
|
XP_011527112.1:p.Pro682Ser
|
|
XM_011528811.2:c.2014C>T
|
XP_011527113.1:p.Pro672Ser
|
|
XM_017027841.2:c.2041C>T
|
XP_016883330.1:p.Pro681Ser
|
|
XM_017027842.2:c.1978C>T
|
XP_016883331.1:p.Pro660Ser
|
|
XM_017027843.1:c.1975C>T
|
XP_016883332.1:p.Pro659Ser
|
|
XM_017027844.2:c.1933C>T
|
XP_016883333.1:p.Pro645Ser
|
|
XM_017027845.1:c.1006C>T
|
XP_016883334.1:p.Pro336Ser
|
|
NM_004518.6:c.1906C>T
|
NP_004509.2:p.Pro636Ser
|
|
NM_172106.3:c.1936C>T
|
NP_742104.1:p.Pro646Ser
|
|
NM_172107.4:c.1990C>T
MANE Select
|
NP_742105.1:p.Pro664Ser
|
|
NM_172108.5:c.1897C>T
|
NP_742106.1:p.Pro633Ser
|
|
NM_001382235.1:c.2044C>T
|
NP_001369164.1:p.Pro682Ser
|
|