ENST00000585124.6:c.1006C>T
MANE Select
|
ENSP00000463999.1:p.Pro336Ser
|
|
ENST00000316199.10:c.1009C>T
|
ENSP00000313950.6:p.Pro337Ser
|
|
ENST00000534871.5:c.883C>T
|
ENSP00000443869.1:p.Pro295Ser
|
|
ENST00000578549.5:c.910C>T
|
ENSP00000462207.1:p.Pro304Ser
|
|
ENST00000584972.5:c.698C>T
|
|
|
ENST00000585124.5:c.1006C>T
|
ENSP00000463999.1:p.Pro336Ser
|
|
NM_001256834.1:c.883C>T
|
NP_001243763.1:p.Pro295Ser
|
|
NM_001256834.2:c.883C>T
|
NP_001243763.1:p.Pro295Ser
|
|
NM_001284526.1:c.1009C>T
|
NP_001271455.1:p.Pro337Ser
|
|
NM_001313950.1:c.1006C>T
|
NP_001300879.1:p.Pro336Ser
|
|
NM_001313951.1:c.883C>T
|
NP_001300880.1:p.Pro295Ser
|
|
NM_001313952.1:c.886C>T
|
NP_001300881.1:p.Pro296Ser
|
|
NM_001313953.1:c.910C>T
|
NP_001300882.1:p.Pro304Ser
|
|
NM_001313954.1:c.550C>T
|
NP_001300883.1:p.Pro184Ser
|
|
NM_001313955.1:c.502C>T
|
NP_001300884.1:p.Pro168Ser
|
|
NM_004217.3:c.1006C>T
|
NP_004208.2:p.Pro336Ser
|
|
NR_132730.1:n.986C>T
|
|
|
NR_132731.1:n.871C>T
|
|
|
XM_011524070.1:c.910C>T
|
XP_011522372.1:p.Pro304Ser
|
|
XM_011524072.1:c.883C>T
|
XP_011522374.1:p.Pro295Ser
|
|
XR_934118.1:n.1215C>T
|
|
|
NM_001313953.2:c.910C>T
|
NP_001300882.1:p.Pro304Ser
|
|
XM_011524072.3:c.883C>T
|
XP_011522374.1:p.Pro295Ser
|
|
XM_017025307.2:c.883C>T
|
XP_016880796.1:p.Pro295Ser
|
|
XM_017025308.2:c.787C>T
|
XP_016880797.1:p.Pro263Ser
|
|
XM_017025309.1:c.550C>T
|
XP_016880798.1:p.Pro184Ser
|
|
XM_017025310.1:c.550C>T
|
XP_016880799.1:p.Pro184Ser
|
|
XM_017025311.1:c.550C>T
|
XP_016880800.1:p.Pro184Ser
|
|
NM_004217.4:c.1006C>T
MANE Select
|
NP_004208.2:p.Pro336Ser
|
|
NM_001256834.3:c.883C>T
|
NP_001243763.1:p.Pro295Ser
|
|
NM_001284526.2:c.1009C>T
|
NP_001271455.1:p.Pro337Ser
|
|
NM_001313950.2:c.1006C>T
|
NP_001300879.1:p.Pro336Ser
|
|
NM_001313952.2:c.886C>T
|
NP_001300881.1:p.Pro296Ser
|
|
NM_001313953.3:c.910C>T
|
NP_001300882.1:p.Pro304Ser
|
|
NM_001313954.2:c.550C>T
|
NP_001300883.1:p.Pro184Ser
|
|
NM_001313955.2:c.502C>T
|
NP_001300884.1:p.Pro168Ser
|
|
NR_132730.2:n.935C>T
|
|
|