ENST00000706989.1:c.2165C>G
|
ENSP00000516702.1:p.Pro722Arg
|
|
ENST00000359125.7:c.2111C>G
MANE Select
|
ENSP00000352035.2:p.Pro704Arg
|
|
ENST00000637193.1:c.1508C>G
|
ENSP00000490734.1:p.Pro503Arg
|
|
ENST00000344462.8:c.2018C>G
|
ENSP00000339611.4:p.Pro673Arg
|
|
ENST00000357249.6:c.1679C>G
|
ENSP00000349789.3:p.Pro560Arg
|
|
ENST00000359125.6:c.2111C>G
|
ENSP00000352035.2:p.Pro704Arg
|
|
ENST00000360480.7:c.2027C>G
|
ENSP00000353668.3:p.Pro676Arg
|
|
ENST00000370224.5:c.2135C>G
|
ENSP00000359244.2:p.Pro712Arg
|
|
ENST00000625514.2:c.2099C>G
|
ENSP00000486040.1:p.Pro700Arg
|
|
ENST00000626839.2:c.2057C>G
|
ENSP00000486706.1:p.Pro686Arg
|
|
ENST00000629241.2:c.2027C>G
|
ENSP00000487142.1:p.Pro676Arg
|
|
ENST00000629676.2:c.1679+6298C>G
|
ENSP00000486194.1:n.1679+6298C>G
|
|
NM_004518.4:c.2027C>G
|
NP_004509.2:p.Pro676Arg
|
|
NM_172106.1:c.2057C>G
|
NP_742104.1:p.Pro686Arg
|
|
NM_172107.2:c.2111C>G
|
NP_742105.1:p.Pro704Arg
|
|
NM_172108.3:c.2018C>G
|
NP_742106.1:p.Pro673Arg
|
|
XM_006723787.1:c.2153C>G
|
XP_006723850.1:p.Pro718Arg
|
|
XM_011528807.1:c.2219C>G
|
XP_011527109.1:p.Pro740Arg
|
|
XM_011528808.1:c.2216C>G
|
XP_011527110.1:p.Pro739Arg
|
|
XM_011528809.1:c.2189C>G
|
XP_011527111.1:p.Pro730Arg
|
|
XM_011528810.1:c.2165C>G
|
XP_011527112.1:p.Pro722Arg
|
|
XM_011528811.1:c.2135C>G
|
XP_011527113.1:p.Pro712Arg
|
|
XM_011528812.1:c.2108C>G
|
XP_011527114.1:p.Pro703Arg
|
|
XM_011528813.1:c.2093C>G
|
XP_011527115.1:p.Pro698Arg
|
|
XM_011528814.1:c.1700C>G
|
XP_011527116.1:p.Pro567Arg
|
|
NM_004518.5:c.2027C>G
|
NP_004509.2:p.Pro676Arg
|
|
NM_172106.2:c.2057C>G
|
NP_742104.1:p.Pro686Arg
|
|
NM_172107.3:c.2111C>G
|
NP_742105.1:p.Pro704Arg
|
|
NM_172108.4:c.2018C>G
|
NP_742106.1:p.Pro673Arg
|
|
XM_011528810.2:c.2165C>G
|
XP_011527112.1:p.Pro722Arg
|
|
XM_011528811.2:c.2135C>G
|
XP_011527113.1:p.Pro712Arg
|
|
XM_017027841.2:c.2162C>G
|
XP_016883330.1:p.Pro721Arg
|
|
XM_017027842.2:c.2099C>G
|
XP_016883331.1:p.Pro700Arg
|
|
XM_017027843.1:c.2096C>G
|
XP_016883332.1:p.Pro699Arg
|
|
XM_017027844.2:c.2054C>G
|
XP_016883333.1:p.Pro685Arg
|
|
XM_017027845.1:c.1127C>G
|
XP_016883334.1:p.Pro376Arg
|
|
NM_004518.6:c.2027C>G
|
NP_004509.2:p.Pro676Arg
|
|
NM_172106.3:c.2057C>G
|
NP_742104.1:p.Pro686Arg
|
|
NM_172107.4:c.2111C>G
MANE Select
|
NP_742105.1:p.Pro704Arg
|
|
NM_172108.5:c.2018C>G
|
NP_742106.1:p.Pro673Arg
|
|
NM_001382235.1:c.2165C>G
|
NP_001369164.1:p.Pro722Arg
|
|